Regenerx Biopharmaceuticals Inc (RGRX) 0.1472 $RGRX
Dr. Michael Chopp Reports on Successful Remodeling of the Central and Peripheral Nervous Systems after Injury/Disease Using Thymosin Beta 4
PR Newswire - Thu Oct 23, 12:00PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTCBB: RGRX) ("the Company" or "RegeneRx"
today reported on data presented by Dr. Michael Chopp at the Fourth International Symposium on Thymosins in Health and Disease in Rome, Italy. Dr. Chopp reviewed research on the use of Thymosin beta 4 (TB4) as a protective and regenerative agent for nervous system injuries and diseases. He also presented data on the molecular mechanisms underlying TB4's therapeutic efficacy, including its modulation of microRNAs and their subsequent multifaceted restorative impact.
RegeneRx to begin Phase 3 study of RGN-259 eye drops in neurotrophic keratopathy patients
M2 - Tue Oct 21, 7:29AM CDT
Therapeutic peptide company RegeneRx Biopharmaceuticals (Other OTC:RGRX) said on Monday that it plans to start its Phase 3 by mid-2015 to evaluate RGN-259 preservative-free eye drops for the treatment of patients with neurotrophic keratopathy (NK), an orphan disease of the cornea, following its September meeting with the US FDA.
RegeneRx Allowed to Proceed with Phase 3 Using RGN-259 Eye Drops for the Treatment of Neurotrophic Keratopathy
PR Newswire - Mon Oct 20, 9:12AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that it met with the FDA in September and as a result of the meeting may begin Phase 3 to evaluate RGN-259 preservative-free eye drops for the treatment of patients with neurotrophic keratopathy (NK), an orphan disease of the cornea. The Company believes clinical trials could be started by mid-2015.
RegeneRx awarded patent for Inhibition or Reversal of Skin Aging in Canada
M2 - Wed Oct 01, 6:07AM CDT
Therapeutic peptide company RegeneRx Biopharmaceuticals (Other OTC :RGRX) revealed on Tuesday the receipt of the Canadian Patent for Inhibition or Reversal of Skin Aging by Actin-Sequestering Peptides.
RegeneRx Receives Canadian Patent for Inhibition or Reversal of Skin Aging
PR Newswire - Tue Sep 30, 9:00AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that it has received a Canadian Patent for Inhibition or Reversal of Skin Aging by Actin-Sequestering Peptides. This patent includes claims using thymosin beta 4, various fragments and analogues, and numerous other actin-sequestering peptides for these purposes. The patent will expire in 2021.
Global Venous Leg Ulcers (Crural ulcer) Therapeutics Pipeline Review 2014 - 11 Companies & 12 Drug Profiles
M2 - Thu Sep 11, 4:32AM CDT
Research and Markets (http://www.researchandmarkets.com/research/hdzqtm/venous_leg_ulcers) has announced the addition of the "Venous Leg Ulcers (Crural ulcer) - Pipeline Review, H2 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Venous Leg Ulcers (Crural ulcer), complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Venous Leg Ulcers (Crural ulcer) and special features on late-stage and discontinued projects. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Companies Involved in Therapeutics Development - Smith & Nephew Plc - CardioVascular BioTherapeutics, Inc. - Stratatech Corporation - RegeneRx Biopharmaceuticals, Inc. - CytoTools AG - FirstString Research, Inc. - CoDa Therapeutics, Inc. - Adocia - Intralytix, Inc. - MacroCure - Pergamum AB Drug Profiles - HP-802247 - CureXcell - Granexin - CVBT-141B - RGN-137 - DermaPro CL-05 - CODA-001 - LL-37 - Stem Cell Therapy for Venous Leg Ulcers - WPP-201 - Biochaperone PDGF-BB - Cathelicidin For more information visit http://www.researchandmarkets.com/research/hd...leg_ulcers
SNN: 32.91 (+1.14)
RegeneRx Receives $1 Million Pursuant to Product License and Stock Purchase Agreement
PR Newswire - Wed Sep 03, 7:45AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that it received a payment of $1 million, representing the last tranche of a $2.5 million product license and securities purchase agreement with G-treeBNT Co., Ltd, to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. G-treeBNT purchased 8,333,333 shares of common stock at $0.12 per share and retains an option until January 31, 2015 to purchase additional common stock for $825,000 at $0.15 per share. The licensing and securities purchase agreements have previously been filed as exhibits to the Company's Quarterly Report on Form 10-Q for the quarter ending March 31, 2014.
Epidermolysis Bullosa - Pipeline Review, H1 2014
M2 - Wed Jul 30, 3:10AM CDT
Research and Markets (http://www.researchandmarkets.com/research/xjhcc9/epidermolysis) has announced the addition of the "Epidermolysis Bullosa - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Epidermolysis Bullosa, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Epidermolysis Bullosa and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. Reasons to buy - Provides strategically significant competitor information, analysis, and insights to formulate effective R&D development strategies - Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage - Develop strategic initiatives by understanding the focus areas of leading companies - Identify and understand important and diverse types of therapeutics under development for Epidermolysis Bullosa - Plan mergers and acquisitions effectively by identifying key players of the most promising pipeline - Devise corrective measures for pipeline projects by understanding Epidermolysis Bullosa pipeline depth and focus of Indication therapeutics - Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope - Modify the therapeutic portfolio by identifying discontinued projects and understanding the factors that drove them from pipeline Companies Mentioned: - RegeneRx Biopharmaceuticals, Inc. - Fibrocell Science, Inc. - Birken AG - Scioderm, Inc. For more information visit http://www.researchandmarkets.com/research/xj...dermolysis
FCSC: 2.88 (-0.02)
New Report: Thymosin B4 Prevents Heart Rupture & Improves Cardiac Function after Heart Attack in Mice
Business Wire - Tue Jul 15, 8:02AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that a new paper entitled, Thymosin B4 Prevents Cardiac Rupture and Improves Cardiac Function in Mice with Myocardial Infarction, was published in the journal, Heart Circulation Physiology, on July 11, 2014. "The present study shows for the first time that 1) TB4 is able to reduce incidence of cardiac rupture post-MI [myocardial infarction or heart attack] and markedly improved cardiac function at 5 weeks after MI, and that 2) the cardiac protective effects of TB4 after MI were associated with a significant reduction of excessive inflammatory response and cardiomyocyte apoptosis as well as with an enhancement of angiogenesis. From a clinical point of view, TB4 could potentially be a therapeutic candidate for patients with acute MI," according to the study's authors.
RegeneRx's Strategic Partner G-treeBNT Preparing for Phase III Dry Eye Trials in Asia with RGN-259
Business Wire - Mon Jul 07, 7:30AM CDT
RegeneRx Pharmaceuticals (OTCBB:RGRX), and G-treeBNT Co. Ltd., a Korean biotech firm, jointly announced today that G-treeBNT is preparing to file an IND and sponsor a Phase III clinical trial with RGN-259 (a Thymosin Beta 4-based preservative-free eye drop) in patients with moderate to severe dry eye initially in South Korea, followed by Japan and Australia, with follow-on registrations in certain additional Asian and Pacific Rim countries if appropriate.
RegeneRx and Lee's Pharmaceutical Dry Eye Drug Progresses - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Mon Jun 23, 11:10AM CDT
RegeneRx Biopharmaceuticals, Inc. (RGRX) and Lee's Pharmaceutical announced that the Chinese regulatory authority has accepted a phase II investigational new drug application for RGN-259.
GILD: 113.45 (+0.86), ALXN: 192.20 (+1.65), REGN: 397.89 (-9.27)
RegeneRx Biopharmaceuticals to begin Phase 2 trial of RGN-259 in dry eye syndrome patients in China in Q1 2015
M2 - Mon Jun 23, 5:25AM CDT
Novel therapeutic company RegeneRx Biopharmaceuticals (Other OTC:RGRX) and Lee's Pharmaceutical Holdings jointly announced on Friday that they will begin the Phase II IND for RGN-259 in patients with moderate to severe dry eye syndrome in China.
Chinese FDA Accepts Phase 2 IND for RGN-259 for Dry Eye
Business Wire - Sun Jun 22, 11:00PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("RegeneRx" and Lee's Pharmaceutical Holdings Ltd. ("Lee's" today jointly announced that the Chinese FDA has accepted a Phase II IND for RGN-259 (thymosin beta 4-based, preservative-free eye drops) to be tested in patients with moderate to severe dry eye syndrome in China.
RegeneRx wins USD1.35m under product license and securities purchase agreement
M2 - Mon Mar 31, 5:42AM CDT
US-based RegeneRx Biopharmaceuticals (Other OTC:RGRX) reported on Friday the receipt of the initial USD1.35m payment pursuant to its product license and securities purchase agreement with G-treeBNT Co headquartered in Gyeonggi-do, Korea
RegeneRx Receives $1.35 Million Pursuant to Product License And Stock Purchase Agreement
Business Wire - Fri Mar 28, 12:27PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that it received the initial $1.35 million payment pursuant to its product license and securities purchase agreement with G-treeBNT Co., Ltd (formerly Digital Aria Co., Ltd.), headquartered in Gyeonggi-do, Korea, for G-treeBNT to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. G-treeBNT purchased stock at $0.12 per share, is obligated to make an additional equity investment of $1.0 million at $0.12 per share by August 31, 2014 and retains an option until January 31, 2015 to purchase additional common stock for $825,000 at $0.15 per share. The licensing and securities purchase agreements will be filed as exhibits to the Company's Quarterly Report on Form 10-Q for the quarter ending March 31, 2014.
RegeneRx and Digital Aria Sign Product License and Stock Purchase Agreements
Business Wire - Fri Mar 07, 6:57AM CST
RegeneRx Biopharmaceuticals, Inc. (OTC:RGRX) ("the Company" or "RegeneRx" today announced that it has entered into two product license agreements with Digital Aria Co., Ltd., headquartered in Gyeonggi-do, Korea, for Digital Aria to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. Digital Aria will also make an equity investment into RegeneRx of $2.35 million enabling RegeneRx to move forward with its ophthalmic clinical program, and retains a 10-month option to purchase additional common stock for $825,000.
RegeneRx Biopharmaceuticals wins patent for Thymosin beta 4 for treating Dry Eye Syndrome in Israel
M2 - Tue Feb 25, 5:44AM CST
Biopharmaceutical company RegeneRx Biopharmaceuticals (Other OTC:RGRX) reported on Monday the receipt of patent for Thymosin beta 4 in Israel.
RegeneRx Receives Israeli Patent for Treatment of Dry Eye Syndrome
Business Wire - Mon Feb 24, 9:00AM CST
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx" today announced that it has received an Israeli patent for the treatment of Dry Eye Syndrome using Thymosin beta 4 (TB4) and various fragments of TB4, as well as other analogues and derivatives. The patent will expire in 2026.
RegeneRx Biopharmaceuticals Inc awarded patent allowance in the US for neuro and muscular degenerative diseases
M2 - Fri Jan 17, 10:38AM CST
RegeneRx Biopharmaceuticals Inc (RGRX) revealed on Thursday that it has received a Notice of Allowance of a US patent application for using novel therapeutic peptide for the prevention and treatment of neuro and muscular degenerative diseases and related tissue damage.
RegeneRx Releases Results of Phase 2 Clinical Trial on Patients with Epidermolysis Bullosa
Business Wire - Mon Jun 24, 7:30AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC Bulletin Board: RGRX) ("the Company" or "RegeneRx" today announced results from its dose-escalating, double-blind, placebo-controlled Phase 2 clinical trial in 30 patients with dystrophic and junctional epidermolysis bullosa (EB), a severe "orphan" skin disorder with limited prevalence in the U.S. and Europe. RGN-137 (a topical formulation of Thymosin beta 4 or TB4) was administered to a single non-healing index lesion in these patients daily for 56 days and followed for an additional 14 days post-treatment.
Dr. Michael Chopp Reports on Successful Remodeling of the Central and Peripheral Nervous Systems after Injury/Disease Using Thymosin Beta 4
PR Newswire - Thu Oct 23, 12:00PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTCBB: RGRX) ("the Company" or "RegeneRx"
today reported on data presented by Dr. Michael Chopp at the Fourth International Symposium on Thymosins in Health and Disease in Rome, Italy. Dr. Chopp reviewed research on the use of Thymosin beta 4 (TB4) as a protective and regenerative agent for nervous system injuries and diseases. He also presented data on the molecular mechanisms underlying TB4's therapeutic efficacy, including its modulation of microRNAs and their subsequent multifaceted restorative impact. RegeneRx to begin Phase 3 study of RGN-259 eye drops in neurotrophic keratopathy patients
M2 - Tue Oct 21, 7:29AM CDT
Therapeutic peptide company RegeneRx Biopharmaceuticals (Other OTC:RGRX) said on Monday that it plans to start its Phase 3 by mid-2015 to evaluate RGN-259 preservative-free eye drops for the treatment of patients with neurotrophic keratopathy (NK), an orphan disease of the cornea, following its September meeting with the US FDA.
RegeneRx Allowed to Proceed with Phase 3 Using RGN-259 Eye Drops for the Treatment of Neurotrophic Keratopathy
PR Newswire - Mon Oct 20, 9:12AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that it met with the FDA in September and as a result of the meeting may begin Phase 3 to evaluate RGN-259 preservative-free eye drops for the treatment of patients with neurotrophic keratopathy (NK), an orphan disease of the cornea. The Company believes clinical trials could be started by mid-2015. RegeneRx awarded patent for Inhibition or Reversal of Skin Aging in Canada
M2 - Wed Oct 01, 6:07AM CDT
Therapeutic peptide company RegeneRx Biopharmaceuticals (Other OTC :RGRX) revealed on Tuesday the receipt of the Canadian Patent for Inhibition or Reversal of Skin Aging by Actin-Sequestering Peptides.
RegeneRx Receives Canadian Patent for Inhibition or Reversal of Skin Aging
PR Newswire - Tue Sep 30, 9:00AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that it has received a Canadian Patent for Inhibition or Reversal of Skin Aging by Actin-Sequestering Peptides. This patent includes claims using thymosin beta 4, various fragments and analogues, and numerous other actin-sequestering peptides for these purposes. The patent will expire in 2021. Global Venous Leg Ulcers (Crural ulcer) Therapeutics Pipeline Review 2014 - 11 Companies & 12 Drug Profiles
M2 - Thu Sep 11, 4:32AM CDT
Research and Markets (http://www.researchandmarkets.com/research/hdzqtm/venous_leg_ulcers) has announced the addition of the "Venous Leg Ulcers (Crural ulcer) - Pipeline Review, H2 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Venous Leg Ulcers (Crural ulcer), complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Venous Leg Ulcers (Crural ulcer) and special features on late-stage and discontinued projects. The report enhances decision making capabilities and help to create effective counter strategies to gain competitive advantage. It strengthens R&D pipelines by identifying new targets and MOAs to produce first-in-class and best-in-class products. Companies Involved in Therapeutics Development - Smith & Nephew Plc - CardioVascular BioTherapeutics, Inc. - Stratatech Corporation - RegeneRx Biopharmaceuticals, Inc. - CytoTools AG - FirstString Research, Inc. - CoDa Therapeutics, Inc. - Adocia - Intralytix, Inc. - MacroCure - Pergamum AB Drug Profiles - HP-802247 - CureXcell - Granexin - CVBT-141B - RGN-137 - DermaPro CL-05 - CODA-001 - LL-37 - Stem Cell Therapy for Venous Leg Ulcers - WPP-201 - Biochaperone PDGF-BB - Cathelicidin For more information visit http://www.researchandmarkets.com/research/hd...leg_ulcers
SNN: 32.91 (+1.14)
RegeneRx Receives $1 Million Pursuant to Product License and Stock Purchase Agreement
PR Newswire - Wed Sep 03, 7:45AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that it received a payment of $1 million, representing the last tranche of a $2.5 million product license and securities purchase agreement with G-treeBNT Co., Ltd, to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. G-treeBNT purchased 8,333,333 shares of common stock at $0.12 per share and retains an option until January 31, 2015 to purchase additional common stock for $825,000 at $0.15 per share. The licensing and securities purchase agreements have previously been filed as exhibits to the Company's Quarterly Report on Form 10-Q for the quarter ending March 31, 2014. Epidermolysis Bullosa - Pipeline Review, H1 2014
M2 - Wed Jul 30, 3:10AM CDT
Research and Markets (http://www.researchandmarkets.com/research/xjhcc9/epidermolysis) has announced the addition of the "Epidermolysis Bullosa - Pipeline Review, H1 2014" report to their offering. This report provides comprehensive information on the therapeutic development for Epidermolysis Bullosa, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Epidermolysis Bullosa and special features on late-stage and discontinued projects. Drug profiles/records featured in the report undergoes periodic updation following a stringent set of processes that ensures that all the profiles are updated with the latest set of information. Additionally, processes including live news & deals tracking, browser based alert-box and clinical trials registries tracking ensure that the most recent developments are captured on a real time basis. Reasons to buy - Provides strategically significant competitor information, analysis, and insights to formulate effective R&D development strategies - Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage - Develop strategic initiatives by understanding the focus areas of leading companies - Identify and understand important and diverse types of therapeutics under development for Epidermolysis Bullosa - Plan mergers and acquisitions effectively by identifying key players of the most promising pipeline - Devise corrective measures for pipeline projects by understanding Epidermolysis Bullosa pipeline depth and focus of Indication therapeutics - Develop and design in-licensing and out-licensing strategies by identifying prospective partners with the most attractive projects to enhance and expand business potential and scope - Modify the therapeutic portfolio by identifying discontinued projects and understanding the factors that drove them from pipeline Companies Mentioned: - RegeneRx Biopharmaceuticals, Inc. - Fibrocell Science, Inc. - Birken AG - Scioderm, Inc. For more information visit http://www.researchandmarkets.com/research/xj...dermolysis
FCSC: 2.88 (-0.02)
New Report: Thymosin B4 Prevents Heart Rupture & Improves Cardiac Function after Heart Attack in Mice
Business Wire - Tue Jul 15, 8:02AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that a new paper entitled, Thymosin B4 Prevents Cardiac Rupture and Improves Cardiac Function in Mice with Myocardial Infarction, was published in the journal, Heart Circulation Physiology, on July 11, 2014. "The present study shows for the first time that 1) TB4 is able to reduce incidence of cardiac rupture post-MI [myocardial infarction or heart attack] and markedly improved cardiac function at 5 weeks after MI, and that 2) the cardiac protective effects of TB4 after MI were associated with a significant reduction of excessive inflammatory response and cardiomyocyte apoptosis as well as with an enhancement of angiogenesis. From a clinical point of view, TB4 could potentially be a therapeutic candidate for patients with acute MI," according to the study's authors. RegeneRx's Strategic Partner G-treeBNT Preparing for Phase III Dry Eye Trials in Asia with RGN-259
Business Wire - Mon Jul 07, 7:30AM CDT
RegeneRx Pharmaceuticals (OTCBB:RGRX), and G-treeBNT Co. Ltd., a Korean biotech firm, jointly announced today that G-treeBNT is preparing to file an IND and sponsor a Phase III clinical trial with RGN-259 (a Thymosin Beta 4-based preservative-free eye drop) in patients with moderate to severe dry eye initially in South Korea, followed by Japan and Australia, with follow-on registrations in certain additional Asian and Pacific Rim countries if appropriate.
RegeneRx and Lee's Pharmaceutical Dry Eye Drug Progresses - Analyst Blog
Zacks Equity Research - Zacks Investment Research - Mon Jun 23, 11:10AM CDT
RegeneRx Biopharmaceuticals, Inc. (RGRX) and Lee's Pharmaceutical announced that the Chinese regulatory authority has accepted a phase II investigational new drug application for RGN-259.
GILD: 113.45 (+0.86), ALXN: 192.20 (+1.65), REGN: 397.89 (-9.27)
RegeneRx Biopharmaceuticals to begin Phase 2 trial of RGN-259 in dry eye syndrome patients in China in Q1 2015
M2 - Mon Jun 23, 5:25AM CDT
Novel therapeutic company RegeneRx Biopharmaceuticals (Other OTC:RGRX) and Lee's Pharmaceutical Holdings jointly announced on Friday that they will begin the Phase II IND for RGN-259 in patients with moderate to severe dry eye syndrome in China.
Chinese FDA Accepts Phase 2 IND for RGN-259 for Dry Eye
Business Wire - Sun Jun 22, 11:00PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("RegeneRx"
and Lee's Pharmaceutical Holdings Ltd. ("Lee's" today jointly announced that the Chinese FDA has accepted a Phase II IND for RGN-259 (thymosin beta 4-based, preservative-free eye drops) to be tested in patients with moderate to severe dry eye syndrome in China. RegeneRx wins USD1.35m under product license and securities purchase agreement
M2 - Mon Mar 31, 5:42AM CDT
US-based RegeneRx Biopharmaceuticals (Other OTC:RGRX) reported on Friday the receipt of the initial USD1.35m payment pursuant to its product license and securities purchase agreement with G-treeBNT Co headquartered in Gyeonggi-do, Korea
RegeneRx Receives $1.35 Million Pursuant to Product License And Stock Purchase Agreement
Business Wire - Fri Mar 28, 12:27PM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that it received the initial $1.35 million payment pursuant to its product license and securities purchase agreement with G-treeBNT Co., Ltd (formerly Digital Aria Co., Ltd.), headquartered in Gyeonggi-do, Korea, for G-treeBNT to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. G-treeBNT purchased stock at $0.12 per share, is obligated to make an additional equity investment of $1.0 million at $0.12 per share by August 31, 2014 and retains an option until January 31, 2015 to purchase additional common stock for $825,000 at $0.15 per share. The licensing and securities purchase agreements will be filed as exhibits to the Company's Quarterly Report on Form 10-Q for the quarter ending March 31, 2014. RegeneRx and Digital Aria Sign Product License and Stock Purchase Agreements
Business Wire - Fri Mar 07, 6:57AM CST
RegeneRx Biopharmaceuticals, Inc. (OTC:RGRX) ("the Company" or "RegeneRx"
today announced that it has entered into two product license agreements with Digital Aria Co., Ltd., headquartered in Gyeonggi-do, Korea, for Digital Aria to develop RegeneRx's RGN-259 preservative-free eye drop product candidate in Asia (excluding China, Hong Kong, Taiwan, and Macau), and its RGN-137 topical dermal gel product candidate in the U.S. Digital Aria will also make an equity investment into RegeneRx of $2.35 million enabling RegeneRx to move forward with its ophthalmic clinical program, and retains a 10-month option to purchase additional common stock for $825,000. RegeneRx Biopharmaceuticals wins patent for Thymosin beta 4 for treating Dry Eye Syndrome in Israel
M2 - Tue Feb 25, 5:44AM CST
Biopharmaceutical company RegeneRx Biopharmaceuticals (Other OTC:RGRX) reported on Monday the receipt of patent for Thymosin beta 4 in Israel.
RegeneRx Receives Israeli Patent for Treatment of Dry Eye Syndrome
Business Wire - Mon Feb 24, 9:00AM CST
RegeneRx Biopharmaceuticals, Inc. (OTC: RGRX) ("the Company" or "RegeneRx"
today announced that it has received an Israeli patent for the treatment of Dry Eye Syndrome using Thymosin beta 4 (TB4) and various fragments of TB4, as well as other analogues and derivatives. The patent will expire in 2026. RegeneRx Biopharmaceuticals Inc awarded patent allowance in the US for neuro and muscular degenerative diseases
M2 - Fri Jan 17, 10:38AM CST
RegeneRx Biopharmaceuticals Inc (RGRX) revealed on Thursday that it has received a Notice of Allowance of a US patent application for using novel therapeutic peptide for the prevention and treatment of neuro and muscular degenerative diseases and related tissue damage.
RegeneRx Releases Results of Phase 2 Clinical Trial on Patients with Epidermolysis Bullosa
Business Wire - Mon Jun 24, 7:30AM CDT
RegeneRx Biopharmaceuticals, Inc. (OTC Bulletin Board: RGRX) ("the Company" or "RegeneRx"
today announced results from its dose-escalating, double-blind, placebo-controlled Phase 2 clinical trial in 30 patients with dystrophic and junctional epidermolysis bullosa (EB), a severe "orphan" skin disorder with limited prevalence in the U.S. and Europe. RGN-137 (a topical formulation of Thymosin beta 4 or TB4) was administered to a single non-healing index lesion in these patients daily for 56 days and followed for an additional 14 days post-treatment. 
