ASX Share rice
Thu 13 May 2021 - 02:13:pm (Sydney)

IGO Share Price

IGO LIMITEDIGOMaterials

IGO Company Information

Name:

IGO Limited

Sector:

Basic Materials

Industry:

Other Industrial Metals & Mining

GIC Industry:

Metals & Mining

GIC Sub Industry:

Diversified Metals & Mining

Address:

South Shore Centre Perth WA Australia 6151

Phone:

61 8 9238 8300

MD, CEO & Exec. Director:

Mr. Peter J. L. Bradford BAppSc, FAusIMM, MSMME, MAIC

Joint Company Sec. & CFO:

Mr. Scott Steinkrug C.A. B.Comm, BSc.

Chief Operating Officer:

Mr. Matt Dusci MAIG

Gen. Counsel:

Ms. Kate Barker

Head of Corp. Devel.:

Mr. Andrew Eddowes B.Sc.

Head of People & Culture:

Ms. Sam Retallack B.Health Sc, CAHRI, DipAppScience

Head of Safety, Health, Environment, Quality (SHEQ) & Risk:

Mr. Keith Ashby B.Sc., M.A.I.C.D., M.Sc.

Gen. Mang. of Exploration:

Mr. Ian Sandl B.Sc.

Company Sec. & Head of Corp. Affairs:

Ms. Joanne McDonald M.Sc., MPA, ACIS

Investor Relations & Communications Mang.:

Richard Glass

Company Overview:

IGO Limited operates as a mining and exploration company in Australia. The company owns a 100% interest in the Nova project, which produces nickel, copper, and cobalt concentrates located to the east-northeast of Norseman; and 30% interest in the Tropicana gold mine covering 3,600 square kilometers of tenements located to the east northeast of Kalgoorlie. It also engages in the exploration of nickel and copper projects located in Western Australia, Northern Territory, and South Australia, as well as Greenland. The company was formerly known as Independence Group NL and changed its name to IGO Limited in January 2020. IGO Limited was founded in 2000 and is headquartered in Perth, Australia.

IGO Share Price Information

Shares Issued:

757.27M

Market Capitalisation:

$5.60B

Dividend per Share:

$0.05

Ex Dividend Date:

2020-09-10

Dividend Yield:

0.68%

Revenue (TTM):

$876.99M

Revenue Per Share (TTM):

$1.47

Earnings per Share:

$0.182

Profit Margin:

0.1245

Operating Margin (TTM):

$0.19

Return On Assets (TTM):

$0.04

Return On Equity (TTM):

$0.05

Quarterly Revenue Growth (YOY):

-0.025

Gross Profit(TTM):

$604.37M

Diluted Earnings Per Share (TTM):

$0.182

QuarterlyEarnings Growth(YOY):

-0.469

IGO CashFlow Statement

CashFlow Date:

2020-06-30

Investments:

$-54,921,000

Change To Liabilities:

$65.54M

Total Cashflow From Investing Activities:

$-115,344,000

Net Borrowings:

$-34,247,000

Net Income:

$155.09M

Total Cash From Operating Activities:

$397.52M

Depreciation:

$244.65M

Other Cashflow From Investing Activities:

$-278,000

Dividends Paid:

$-82,712,000

Change To Inventory:

$-20,713,000

Change To Account Receivables:

$-21,215,000

Capital Expenditures:

$87.67M

IGO Income Statement

Income Date:

2020-06-30

Income Before Tax:

$219.51M

Net Income:

$155.09M

Gross Profit:

$604.37M

Operating Income:

$187.01M

Other Operating Expenses:

$14.52M

Interest Expense:

$3.55M

Income Tax Expense:

$64.42M

Total Revenue:

$888.93M

Cost Of Revenue:

$284.56M

IGO Balance Sheet

Balance Sheet Date:

2020-06-30

Total Liabilities:

$367.22M

Total Stockholder Equity:

$1.93B

Total Assets:

$2.29B

Common Stock:

$1.90B

Other Current Assets:

$64K

Retained Earnings:

$9.81M

Other Liabilities:

$210.43M

Other Assets:

$187.93M

Cash:

$510.31M

Total Current Liabilities:

$123.24M

Property - Plant & Equipment:

$1.34B

Net Tangible Assets:

$1.93B

Total Current Assets:

$762.87M

Net Receivables:

$65.91M

Short-Term Investments:

$1.53B

Inventory:

$75.67M

Accounts Payable:

$53.01M

Non Currrent Assets (Other):

$67.91M

Short-Term Investments:

$1.53

Non Current Liabilities Total:

$243.98M

IGO Share Price History

IGO News

26 Apr, 2021
Does the April share price for IGO Limited ( ASX:IGO ) reflect what it's really worth? Today, we will estimate the...
02 Mar, 2021
LAWRENCEVILLE, N.J., March 02, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), a clinical-stage development company focused on DNA-based immunotherapy and next-generation vaccines, today announced that a poster on the Company’s Phase I/II OVATION 2 Study with GEN-1 in advanced ovarian cancer has been accepted for presentation at the Virtual Annual Meeting on Women’s Cancer, sponsored by the Society of Gynecologic Oncology. The conference is being held March 19-25, 2021. The OVATION 2 Study design is being presented as a poster entitled “A Phase I/II Study Evaluating Intraperitoneal GEN-1 in Combination with Neoadjuvant Chemotherapy in Patients with Newly Diagnosed Advanced Epithelial Ovarian Cancer (EOC)” in the “Trials in Progress” poster session from March 19 to 25 (8 pm to 11 pm each day). GEN-1 is Celsion’s DNA-mediated interleukin-12 (IL-12) immunotherapy designed using TheraPlas, its proprietary, synthetic, non-viral nanoparticle delivery system platform. Poster authors are: P.H. Thaker, R.W. Holloway, L. Kuroki, S. E. DePasquale, W.H. Bradley, A. ElNaggar, M.C. Bell, R.P. Rocconi, A. Bregar, M.D. Indermaur, C. Gunderson, B. Pothuri, R. Agajanian, D. Warshal, D. Provencher, M. McHale, V. John, M. Bergman, S. Lau, L. Musso, K. Anwer, N. Borys, C.A. Leath III and the poster will be available for virtual viewing during the meeting. “We are delighted that the Society of Gynecologic Oncology has accepted this poster for presentation,” said Michael H. Tardugno, Celsion’s chairman, president and chief executive officer. “The poster authors, led by the Study Chair of the OVATION 2 Study Dr. Premal Thaker of Washington University School of Medicine in St. Louis, are a Who’s Who of key opinion leaders in women’s health. Celsion is grateful to have such luminaries represent our study to their peers.” The poster describes the OVATION 2 Study, which combines GEN-1 with standard-of-care neoadjuvant chemotherapy (NACT) in patients newly diagnosed with Stage III/IV ovarian cancer. NACT is designed to shrink the cancer as much as possible for optimal surgical removal after three cycles of chemotherapy. Following NACT, patients undergo interval debulking surgery, followed by three adjuvant cycles of chemotherapy and up to nine additional weekly GEN-1 treatments, the goal of which is to delay progression and improve overall survival. The OVATION 2 Study is an open-label, 1-to-1 randomized trial, 80% powered to show the equivalent of a 33% improvement in progression-free survival (PFS) (HR=0.75), the primary endpoint, when comparing the treatment arm (standard of care + GEN-1) with the control arm (standard of care alone). The poster will be available https://investor.celsion.com/scientific-presentations on March 19, 2021. The Company recently announced that to date it has enrolled approximately one-third, or 34 patients, of the anticipated 110 patients to be enrolled into the OVATION 2 Study, of which 20 are in the treatment arm and 14 are in the control. Currently, 28 patients have had their interval debulking surgery with the following results: 13 of 16, or 81%, of patients treated with GEN-1 had a R0 resection, which indicates a microscopically margin-negative complete resection in which no gross or microscopic tumor remains in the tumor bed.7 of 12 patients, or 58%, of patients in the control arm had an R0 resection.This interim data represents a 40% improvement in R0 resection rates for GEN-1- patients compared with control arm patients and is consistent with the reported improvement in resection scores noted in the encouraging Phase I OVATION 1 Study, the manuscript of which has been submitted for peer review publication. Celsion also announced last week that GEN-1 had received Fast Track designation from the U.S. Food and Drug Administration (FDA). This designation is intended to facilitate the development and expedite the regulatory review of drugs to treat serious conditions and fill an unmet medical need. About GEN-1 Immunotherapy GEN-1, designed using Celsion's proprietary TheraPlas platform technology, is an IL-12 DNA plasmid vector encased in a nanoparticle delivery system, which enables cell transfection followed by persistent, local secretion of the IL-12 protein. IL-12 is one of the most active cytokines for the induction of potent anti-cancer immunity acting through the induction of T-lymphocyte and natural killer (NK) cell proliferation. The Company has previously reported positive safety and encouraging Phase I results with GEN-1 given as monotherapy or a combination therapy in patients with advanced peritoneally metastasized primary or recurrent ovarian cancer, and recently completed a Phase Ib dose-escalation trial (OVATION 1 Study) of GEN-1 in combination with carboplatin and paclitaxel in patients with newly diagnosed ovarian cancer. About the Virtual Annual Meeting on Women’s Cancer The Society of Gynecologic Oncology (SGO) 2021 Annual Meeting on Women’s Cancer will be a fully virtual meeting, allowing participants to access high-quality content and engage remotely from around the world in a platform that will be designed explicitly for this meeting. SGO is working hard to provide a great virtual experience with the latest gynecologic cancer research and education you have come to expect at the Annual Meeting on Women’s Cancer. All education sessions will be recorded and available through the virtual platform for attendees who register for the meeting by March 25, 2021. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including immunotherapies and DNA-based therapies; and a platform for the development of nucleic acid vaccines currently focused on SARS-CoV2. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Forward-looking Statements Forward-looking statements in this news release are made pursuant to the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including, unforeseen changes in the course of research and development activities and in clinical trials; the uncertainties of and difficulties in analyzing interim clinical data, particularly in small subgroups that are not statistically significant; FDA and regulatory uncertainties and risks; the significant expense, time and risk of failure of conducting clinical trials; the need for Celsion to evaluate its future development plans; possible acquisitions or licenses of other technologies, assets or businesses; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in the Celsion's periodic filings with the Securities and Exchange Commission. Celsion assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
01 Mar, 2021
The most you can lose on any stock (assuming you don't use leverage) is 100% of your money. But on the bright side, if...
26 Feb, 2021
LAWRENCEVILLE, N.J., Feb. 26, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), a clinical-stage development company focused on DNA-based immunotherapy and next-generation vaccines, today announced that management will be holding one-on-one meetings with investors during the Virtual 33rd Annual Roth Conference, being held March 15 – 17, 2021. A webcast of Celsion’s presentation will be pre-recorded and will be available on the Company’s website during the week before the conference. Institutional and other investors interested in meeting with Celsion during the conference should contact their Roth Capital Partners sales representative or LHA Investor Relations. Conference information is available at www.roth.com/oc2021virtual. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including immunotherapies, DNA-based therapies and directed chemotherapies through clinical trials and eventual commercialization. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
Despite the recent market-wide pullback, oncology drug-maker Celsion (CLSN) is enjoying a breakout year, with shares up by 210% year-to-date. One Street analyst thinks the stock has a way to run yet. Brookline Capital analyst Kumaraguru Raja reiterated a Buy rating on CLSN shares, while boosting his price target from $3 to $4. The new figure implies an 82% upside from current levels. (To watch Raja’s track record, click here) So, what is Raja basing his confident take on? On Monday, Celsion disclosed that the FDA has granted Fast Track designation for GEN-1, the company's potential treatment for advanced ovarian cancer. The DNA-mediated interleukin-12 (IL-12) immunotherapy has concluded a Phase 1b trial and paired with chemotherapy is currently being studied in a Phase 2 trial. The treatment is derived from Celsion’s proprietary, synthetic, non-viral nanoparticle delivery system platform TheraPlas. Fast Track status is not lightly granted and only given to treatments that fill an unmet medical need and which have shown to have an advantage over available therapies. Additionally, they provide better access to the FDA and help speed up development. The FDA were evidently impressed with the Phase 1 data which showed that in seven out of eight patients (88%) GEN-1 led to complete tumor resection. In contrast, standard-of-care neoadjuvant chemotherapy on its own, displayed a 50% resection rate. In line with a new price target, Raja made other adjustments to his Celsion model following the latest news. “We are increasing the probability of success for GEN-1 in ovarian cancer to 60% and add pipeline premium to account for potential of PLACCINE DNA vaccine platform technology,” the 5-star analyst said. “We assume 20% peak penetration and assume a cost of treatment $60,000 per year on launch in 2024.” Celsion exited 3Q20 with $18.3 million of cash in the coffers and last month raised $32.6 million in net proceeds from a stock offering. The strengthened balance sheet is expected to fund operations into next year, according to Raja. “The company expects to manage expenses so that they are able to complete the Phase 2 OVATION study,” Raja summed up. Celsion appears to be flying under the Street’s radar and currently Raja's is the sole recent Celsion review. (See CLSN stock analysis on TipRanks) To find good ideas for healthcare stocks trading at attractive valuations, visit TipRanks’ Best Stocks to Buy, a newly launched tool that unites all of TipRanks’ equity insights. Disclaimer: The opinions expressed in this article are solely those of the featured analyst. The content is intended to be used for informational purposes only. It is very important to do your own analysis before making any investment.
25 Feb, 2021
Of 27 patients who completed interval debulking surgery, 80% of those treated with GEN-1 had an R0 resection compared with 58% of control patients, a 38% improvement To date 34 patients, or approximately one-third of the total, have been enrolled at 22 sites, including 20 patients in the treatment arm and 14 patients in the control arm LAWRENCEVILLE, N.J., Feb. 25, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), a clinical-stage development company focused on DNA-based immunotherapy and next-generation vaccines, today provided an update on its Phase I/II OVATION 2 Study with GEN-1 in patients with advanced ovarian cancer, including interim observations. GEN-1 is Celsion’s DNA-mediated interleukin-12 (IL-12) immunotherapy designed using TheraPlas, its proprietary, synthetic, non-viral nanoparticle delivery system platform. The OVATION 2 Study combines GEN-1 with standard-of-care neoadjuvant chemotherapy (NACT) in patients newly diagnosed with Stage III/IV ovarian cancer. NACT is designed to shrink the cancer as much as possible for optimal surgical removal after three cycles of chemotherapy. Following NACT, patients undergo interval debulking surgery, followed by three adjuvant cycles of chemotherapy and up to nine additional weekly GEN-1 treatments, the goal of which is to delay progression and improve overall survival. The OVATION 2 Study is an open-label, 1-to-1 randomized trial, 80% powered to show the equivalent of a 33% improvement in progression-free survival (PFS) (HR=0.75), the primary endpoint, when comparing the treatment arm (standard of care + GEN-1) with the control arm (standard of care alone). To date, the Company has enrolled approximately one-third, or 34 patients, of the anticipated 110 patients to be enrolled into the OVATION 2 Study, of which 20 are in the treatment arm and 14 are in the control. Currently, 27 patients have had their interval debulking surgery with the following results: 12 of 15, or 80%, of patients treated with GEN-1 had a R0 resection, which indicates a microscopically margin-negative complete resection in which no gross or microscopic tumor remains in the tumor bed.7 of 12 patients, or 58%, of patients in the control arm had an R0 resection.This interim data represents a 38% improvement in R0 resection rates for GEN-1- patients compared with control arm patients and is consistent with the reported improvement in resection scores noted in the encouraging Phase I OVATION I Study, the manuscript of which has been submitted for peer review publication. “As the goal for surgical debulking is to eliminate microscopic disease, more ovarian cancer patients require neoadjuvant chemotherapy. However, little progress has been made in adding additional efficacious immunotherapy agents to standard neoadjuvant chemotherapy,” said Premal H. Thaker, M.D., MSc., Professor in Gynecologic Oncology and Director of Gynecologic Oncology Clinical Research at Washington University School of Medicine in St. Louis and lead Principal Investigator for the OVATION 2 Study. “The results seen to date in the OVATION 2 Study are exciting and impactful for ovarian cancer patients.” The Company further reports that 22 clinical sites in the U.S. and Canada have been initiated, with three more sites expected to be added by the end of the first quarter. Clinical investigators met in early February in a virtual meeting and expressed excitement about the potential for GEN-1 to treat advanced ovarian cancer and, despite the challenges and earlier delays posed by the COVID-19 pandemic, they remain committed to completing enrollment in the study during the second half of 2021. Commenting on the interim patient reports, Dr. Nick Borys, chief medical officer of Celsion, said, “We are gratified that such a high proportion of GEN-1 patients had no residual disease at the time of their debulking surgery. These results are consistent with what we observed in our Phase I (OVATION I) study. This is great news for the patients and the surgeons in our study as a R0 resection suggests a good clinical outcome. We are following our patients carefully to see how well they do long term. The OVATION 2 investigators remain enthusiastic about the potential of GEN-1 to treat late-stage ovarian cancer, which currently has few treatment options.” Celsion announced earlier this week that GEN-1 had received Fast Track designation from the U.S. Food and Drug Administration (FDA). This designation is intended to facilitate the development and expedite the regulatory review of drugs to treat serious conditions and fill an unmet medical need. According to the FDA, a Fast Track Drug must show some advantage over available therapy, including: Showing superior effectiveness, effect on serious outcomes or improved effect on serious outcomesAvoiding serious side effects of an available therapyDecreasing a clinically significant toxicity of an available therapy that is common and causes discontinuation of treatment About GEN-1 Immunotherapy GEN-1, designed using Celsion's proprietary TheraPlas platform technology, is an IL-12 DNA plasmid vector encased in a nanoparticle delivery system, which enables cell transfection followed by persistent, local secretion of the IL-12 protein. IL-12 is one of the most active cytokines for the induction of potent anti-cancer immunity acting through the induction of T-lymphocyte and natural killer (NK) cell proliferation. The Company has previously reported positive safety and encouraging Phase I results with GEN-1 given as monotherapy or a combination therapy in patients with advanced peritoneally metastasized primary or recurrent ovarian cancer, and recently completed a Phase Ib dose-escalation trial (OVATION 1 Study) of GEN-1 in combination with carboplatin and paclitaxel in patients with newly diagnosed ovarian cancer. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including immunotherapies and DNA-based therapies; and a platform for the development of nucleic acid vaccines currently focused on SARS-CoV2. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Forward-looking Statements Forward-looking statements in this news release are made pursuant to the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including, unforeseen changes in the course of research and development activities and in clinical trials; the uncertainties of and difficulties in analyzing interim clinical data, particularly in small subgroups that are not statistically significant; FDA and regulatory uncertainties and risks; the significant expense, time and risk of failure of conducting clinical trials; the need for Celsion to evaluate its future development plans; possible acquisitions or licenses of other technologies, assets or businesses; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in the Celsion's periodic filings with the Securities and Exchange Commission. Celsion assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
23 Feb, 2021
Non-Dilutive Funding Strengthens Balance Sheet; Extends Current Operating Runway to Over Three Years LAWRENCEVILLE, N.J., Feb. 23, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), a clinical stage development company focused on DNA based immunotherapy and next generation vaccines, today announced it has received approval from the New Jersey Economic Development Authority’s (NJEDA) Technology Business Tax Certificate Transfer (NOL) program to sell $2 million of its unused New Jersey net operating losses (NOLs) for the tax years 2018 and 2019. The NOLs are typically sold at a small, single-digit discount to qualified companies with operations in New Jersey. As a result, the Company anticipates it will be able to transfer this credit and receive approximately $1.85 million of net cash proceeds. With this additional funding, the Company expects to report over $54 million in cash and investments at end of the first quarter ending March 31, 2021. This competitive program, administered by the NJEDA, enables qualified companies to sell their unused New Jersey net operating losses and R&D tax credits to unaffiliated, profit-generating corporate taxpayers in the state of New Jersey, up to a current maximum lifetime benefit of $15 million per company. This allows technology and biotechnology companies with NOLs to turn their tax losses and credits into cash proceeds to fund more R&D, expand its workforce, and cover other allowable expenditures. Celsion was one of several qualifying biotechnology/technology companies to share in the funding this year. “The NJEDA’s NOL program reinforces our belief in the State of New Jersey’s commitment to biotechnology research. With the New Jersey State Legislature increasing the maximum lifetime benefit per company from $15 million to $20 million, we plan to participate in this innovative funding program again next year,” said Michael H. Tardugno, Celsion Corporation’s chairman, president and chief executive officer. “The proceeds from the NOL sale helps augment our cash position, and together with the recent $35 million common stock only financing in January 2021, at the current spending rate, extends our operating runway into the first quarter of 2024. With this new, non-dilutive funding, we are positioned to continue to advance our recently announced vaccine initiative. Additionally, we expect these funds to cover full patient enrollment and primary efficacy read-out of the Phase I/II OVATION 2 Study for GEN-1, depending upon the extent to which Progression Free Survival (PFS) is achieved. We appreciate the support and commitment of the NJEDA in facilitating our continued innovation and applaud their efforts to foster continued investment and growth for businesses in New Jersey.” “Throughout the course of 2020 and into the first quarter of 2021, Celsion has sought innovative ways to finance our clinical development programs in some of the world’s most challenging cancers. Balancing the high cost of research and drug development without losing focus on our shareholders is reflected in our successful application to sell $15 million of our New Jersey NOL’s over the past three years,” said Jeffrey W. Church, Celsion Corporation’s Executive Vice President and CFO. “With the support of our shareholders, we look forward to an exciting and promising year ahead.” For more details on this funding for this year’s NOL program, please visit www.njeda.com. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including DNA-based immunotherapies and next generation vaccines, through clinical trials and eventual commercialization. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. PLACCINE, a non-clinical stage DNA plasmid vaccine platform, is in early development with its first application targeting SARS-CoV-2. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Forward-looking Statements Forward-looking statements in this news release are made pursuant to the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including, unforeseen changes in the course of research and development activities and in clinical trials; the uncertainties of and difficulties in analyzing interim clinical data, particularly in small subgroups that are not statistically significant; FDA and regulatory uncertainties and risks; the significant expense, time and risk of failure of conducting clinical trials; the need for Celsion to evaluate its future development plans; possible acquisitions or licenses of other technologies, assets or businesses; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in the Celsion's periodic filings with the Securities and Exchange Commission. Celsion assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
22 Feb, 2021
Celsion’s Commitment to Promoting Immune System Solutions to Fight Life-Threatening Diseases Granted an Accelerated Development Pathway Designation Provides Potential for an Expedited Regulatory Review. LAWRENCEVILLE, N.J., Feb. 22, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), a clinical stage development company focused on DNA based immunotherapy and next generation vaccines, today announced that it has received Fast Track designation from the U.S. Food and Drug Administration (FDA) for GEN-1, its DNA-mediated interleukin-12 (IL-12) immunotherapy currently in Phase II development for the treatment of advanced ovarian cancer. GEN-1 was designed using TheraPlas, Celsion's proprietary, synthetic, non-viral nanoparticle delivery system platform. Fast Track designation is intended to facilitate the development and expedite the regulatory review of drugs to treat serious conditions and fill an unmet medical need. According to the FDA, a Fast Track Drug must show some advantage over available therapy, including: Showing superior effectiveness, effect on serious outcomes or improved effect on serious outcomesAvoiding serious side effects of an available therapyDecreasing a clinical significant toxicity of an available therapy that is common and causes discontinuation of treatment “Fast Track designation is an important step in developing GEN-1 for advanced ovarian cancer. Presuming the encouraging data we are generating in early clinical studies continues, this designation supports an expedited path to market,” said Michael H. Tardugno, Celsion’s chairman, president and chief executive officer. “Fast Track allows for more frequent communication with the FDA to discuss development plans and clinical trial design. In addition, should criteria be met, Fast Track-designated drugs are eligible for rolling review, a process whereby the drug’s sponsor can separately submit sections of its New Drug Application to the FDA. They also are eligible for accelerated approval and priority review, under which drugs for serious conditions fulfilling an unmet medical need can be approved based on a surrogate endpoint. We are optimistic that GEN-1 represents a game-changer for women with advanced ovarian cancer who have limited treatment options.” GEN-1 is the subject of Celsion’s Phase II OVATION 2 Study, which combines GEN-1 with standard-of-care neoadjuvant chemotherapy (NACT) in patients newly diagnosed with Stage III/IV ovarian cancer. NACT is designed to shrink the cancer as much as possible for optimal surgical removal after three cycles of chemotherapy. Following NACT, patients undergo interval debulking surgery, followed by three adjuvant cycles of chemotherapy and up to nine additional weekly GEN-1 treatments, the goal of which is to delay progression and improve overall survival. The OVATION 2 Study is an open-label, 1-to-1 randomized trial, 80% powered to show the equivalent of a 33% improvement in progression-free survival (PFS) (HR=0.75), the primary endpoint, when comparing the treatment arm (standard of care + GEN-1) with the control arm (standard of care alone). As Celsion has previously announced, it has shared with the FDA data from the Phase I portion of the Phase I/II OVATION 2 Study that showed successful tumor resections, with seven out of eight patients (88%) in the GEN-1 treatment arm having a complete tumor resection (R0), which indicates a microscopically margin-negative resection in which no gross or microscopic tumor remains in the tumor bed. The NACT-only treatment arm had an R0 resection rate of 50%. Patients in the Company’s completed Phase 1b dose-escalation OVATION I Study showed compelling objective response rates, with 100% of patients in high-dose cohorts experiencing a complete or partial response, and 67% of patients in lower-dose cohorts experiencing a complete or partial response. Further, R0 resections in the high-dose cohorts was 88%, compared with 33% in the low-dose cohorts. In addition, Celsion compared matched patient data in a synthetic control arm with results from the OVATION I Study. Patients in the GEN-1 arm virtually demonstrated a doubling of control of their cancer compared with the synthetic control arm. Findings are not statistically significant due to the small number of patients. This comparison showed positive data in progression-free survival (PFS) as follows: GEN-1 PopulationPFS Hazard Ratio (Confidence Interval)Intent-to-treat, n=150.53 (95% CI 0.16, 1.73); log-rank p=0.29Per-protocol, n=140.33 (95% CI 0.08, 1.37); log-rank p=0.11 About GEN-1 Immunotherapy GEN-1, designed using Celsion's proprietary TheraPlas platform technology, is an IL-12 DNA plasmid vector encased in a nanoparticle delivery system, which enables cell transfection followed by persistent, local secretion of the IL-12 protein. IL-12 is one of the most active cytokines for the induction of potent anti-cancer immunity acting through the induction of T-lymphocyte and natural killer (NK) cell proliferation. The Company has previously reported positive safety and encouraging Phase I results with GEN-1 given as monotherapy or a combination therapy in patients with advanced peritoneally metastasized primary or recurrent ovarian cancer, and recently completed a Phase Ib dose-escalation trial (OVATION I Study) of GEN-1 in combination with carboplatin and paclitaxel in patients with newly diagnosed ovarian cancer. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including immunotherapies and DNA-based therapies; and a platform for the development of nucleic acid vaccines currently focused on SARS-CoV2. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Forward-looking Statements Forward-looking statements in this news release are made pursuant to the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including, unforeseen changes in the course of research and development activities and in clinical trials; the uncertainties of and difficulties in analyzing interim clinical data, particularly in small subgroups that are not statistically significant; FDA and regulatory uncertainties and risks; the significant expense, time and risk of failure of conducting clinical trials; the need for Celsion to evaluate its future development plans; possible acquisitions or licenses of other technologies, assets or businesses; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in the Celsion's periodic filings with the Securities and Exchange Commission. Celsion assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
12 Feb, 2021
Board to provide guidance in developing the PLACCINE platform for the prevention and treatment of infectious agents, including SARS-CoV-2 LAWRENCEVILLE, N.J., Feb. 12, 2021 (GLOBE NEWSWIRE) -- Celsion Corporation (NASDAQ: CLSN), an oncology drug development company, today announced the formation of a Vaccine Advisory Board and the appointment of its first two members: Britt A. Glaunsinger, Ph.D., Professor, Virology & Molecular Biology, Howard Hughes Medical Institute, University of California, Berkeley, and Dr. Xinzhen Yang, M.D., Ph.D., Independent Professional Consultant for the Gerson Lehman Group and former Director of Viral Vaccines / Program Lead of the HCMV Vaccine Program at Pfizer Inc. “We are delighted to launch our Vaccine Advisory Board with these impressive scientists as charter members,” said Michael H. Tardugno, Celsion’s chairman, president and chief executive officer. “We view Drs. Glaunsinger’s and Yang’s agreement to advise us on the development of our TheraPlas technology-based PLACCINE DNA vaccine platform for the prevention and treatment of COVID-19 and other dangerous viruses as a vote of confidence in our technology. We look forward to adding more talented individuals to this advisory board, as well as to making key internal hires as we advance this promising platform.” With more than 20 years of academic experience in microbiology and virology, Dr. Glaunsinger has held research positions and professorships at the University of California, San Francisco, Howard Hughes Medical Institute and the University of California, Berkeley (with tenure), where she holds the UC Berkeley Class of 1963 Endowed Chair. In recent years, she served as Vice Chair, Gordon Conference on Viruses and Cells; Member of the 2020 COVID-19 Rapid Research Response Scientific Advisory Board, Innovative Genomics Institute; Member of the advisory board of the 2020 COVID-19 Catalyst Fund; Chair of the 2020 Center for Emerging and Neglected Diseases; and, Chair of the 2021 Gordon Conference on Viruses and Cells. A prolific researcher, Dr. Glaunsinger has published more than 60 peer-reviewed articles on viruses. Dr. Glaunsinger earned a B.S. in molecular and cell biology from the University of Arizona, a Ph.D. in molecular virology from the Baylor College of Medicine and was a postdoctoral research fellow at the University of California, San Francisco. She is a lifetime member of the American Society for Virology, and is a member of the American Society for Microbiology and the RNA Society. Dr. Yang has global experience leading cross-functional teams to develop products from scientific discovery to preclinical to clinical evidence development. He has advanced expertise in virology, vaccinology and immunology with extensive research and teaching experience in leading institutions in academia and in the pharmaceutical industry. He currently serves as a consultant for the Gerson Lehman Group. Previously, Dr. Yang joined Pfizer in 2014 and held positions of increasing responsibility, serving as Director, Viral Vaccines and Program Lead of The HCMV (human cytomegalovirus) Vaccine program. At Pfizer he served as a member of the Vaccine Technical Review Committee and as a member of Vaccine Clinical Review Committee. Previously he served on the faculty of the Chinese Academy of Preventive Medicine, where he led pioneering epidemiological studies on HIV/AIDS in China. Dr. Yang has published many peer-reviewed articles. Dr. Yang earned an M.S. in epidemiology and holds the M.D. degree equivalent from Fudan University (formerly the Shanghai Medical University) and a Ph.D. in Molecular Virology from Baylor College of Medicine. He was a postdoctoral research fellow at Harvard Medical School, where he also was an Instructor of Pathology and Assistant Professor of Medicine and Virology. About the PLACCINE platform PLACCINE is Celsion’s proprietary plasmid and DNA delivery technology and the subject of a provisional patent application that covers a broad range of next-generation DNA vaccines and was announced on January 28, 2021. An adaptation of the Company’s TheraPlas technology, PLACCINE is a DNA vaccine technology platform characterized by a single plasmid DNA with multiple coding regions. The plasmid vector is designed to express multiple pathogen antigens along with a potent immune modifier. It is delivered via a synthetic delivery system and has the potential to be easily modified to create vaccines against a multitude of infectious diseases, addressing: Viral Mutations: PLACCINE may offer broad-spectrum and mutational resistance (variants) by targeting multiple antigens on a single plasmid vector.Enhanced Efficacy: The potent immune modifier IL-12 may improve humoral and cellular responses to viral antigens and can be incorporated in the plasmid.Durable Efficacy: PLACCINE delivers a DNA plasmid-based antigen that can result in durable antigen exposure and a robust vaccine response to viral antigens.Storage & Distribution: PLACCINE allows for stability that is compatible with manageable vaccine storage and distribution.Dosing & Administration: PLACCINE is a synthetic delivery system that should require a simple injection that does not require viruses or special equipment to deliver its payload. About Celsion Corporation Celsion is a fully integrated, clinical stage biotechnology company focused on advancing a portfolio of innovative cancer treatments, including immunotherapies, DNA-based therapies and directed chemotherapies through clinical trials and eventual commercialization. The company’s product pipeline includes GEN-1, a DNA-based immunotherapy for the localized treatment of ovarian cancer. ThermoDox®, a proprietary heat-activated liposomal encapsulation of doxorubicin, is under investigator-sponsored development for several cancer indications. Celsion also has two feasibility stage platform technologies for the development of novel nucleic acid-based immunotherapies and other anti-cancer DNA or RNA therapies. Both are novel synthetic, non-viral vectors with demonstrated capability in nucleic acid cellular transfection. For more information on Celsion, visit www.celsion.com. Forward-looking Statements Forward-looking statements in this news release are made pursuant to the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are based upon current beliefs, expectation, and assumptions and include statements regarding the platform having the potential to provide broad protection against coronavirus disease 2019 (COVID-19), and possible future mutations of SARS-CoV-2 or other coronaviruses. These statements are subject to a number of risks and uncertainties, many of which are difficult to predict, including the ability of the Company’s platform to provide broad protection against COVID-19, and possible future mutations of SARS-CoV-2 or other coronaviruses, the issuance of a patent to the Company for use of its technology platform for treating or preventing infection with the SARS-CoV-2 virus that causes COVID-19, unforeseen changes in the course of research and development activities and in clinical trials; the uncertainties of and difficulties in analyzing interim clinical data, particularly in small subgroups that are not statistically significant; FDA and regulatory uncertainties and risks; the significant expense, time and risk of failure of conducting clinical trials; the need for Celsion to evaluate its future development plans; possible acquisitions or licenses of other technologies, assets or businesses; possible actions by customers, suppliers, competitors or regulatory authorities; and other risks detailed from time to time in the Celsion's periodic filings with the Securities and Exchange Commission. Celsion assumes no obligation to update or supplement forward-looking statements that become untrue because of subsequent events, new information or otherwise. Celsion Investor ContactJeffrey W. ChurchExecutive Vice President and CFO609-482-2455jchurch@celsion.com LHA Investor RelationsKim Sutton Golodetz212-838-3777kgolodetz@lhai.com # # #
06 Feb, 2021
22:16
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IGO Dividend Payments

EX-Date Dividend Amount
2010-03-02$0.0197
2010-09-09$0.0296
2011-03-03$0.0396
2011-09-09$0.0297
2012-03-06$0.0198
2012-09-12$0.0099
2013-03-13$0.0099
2013-09-06$0.0099
2014-03-05$0.0297
2014-09-12$0.0495
2015-03-04$0.0594
2015-09-28$0.0247
2016-09-07$0.0198
2017-03-09$0.0099
2017-09-06$0.0099
2018-03-12$0.0099
2018-09-13$0.0198
2019-02-14$0.0198
2019-09-12$0.0792
2020-02-13$0.0594
2020-09-10$0.0495

IGO Dividends (last 11 Years)