Y-mAbs Announces Pipeline Update
By Dr. Matthew Watson
NEW YORK, Dec. 16, 2020 (GLOBE NEWSWIRE) -- Y-mAbs Therapeutics, Inc. (the “Company” or “Y-mAbs”) (Nasdaq: YMAB) a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer, today announced that data for DANYELZA® (naxitamab-gqgk), omburtamab and nivatrotamab will be presented at the Company’s R&D event, which takes place virtually today at 12 p.m. Eastern Time. Key opinion leaders, including Shakeel Modak, M.D., MRCP, Memorial Sloan Kettering (“MSK”), Jaume Mora, M.D., Ph.D., SJD Barcelona Children's Hospital, and Brian H. Santich, Ph.D., MSK, will discuss the current treatment landscape and unmet medical needs for high-risk neuroblastoma, osteosarcoma and other solid tumors. Investors, analysts, members of the media and public may access the event via a live webcast.
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Y-mAbs Announces Pipeline Update
BioSyent Launches Combogesic®, First-Ever Acetaminophen + Ibuprofen Combination Tablet in Canada Now Available
By Dr. Matthew Watson
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BioSyent Launches Combogesic®, First-Ever Acetaminophen + Ibuprofen Combination Tablet in Canada Now Available
Emerging Markets Report: Doctor’s Orders
By Dr. Matthew Watson
An Emerging Markets News Commentary An Emerging Markets News Commentary
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Emerging Markets Report: Doctor’s Orders
AB Science will host a live webcast on December 17, 2020 on masitinib results in Alzheimer’s Disease
By Dr. Matthew Watson
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AB Science will host a live webcast on December 17, 2020 on masitinib results in Alzheimer’s Disease
Chimeric antigen receptor (CAR)-modified cytokine induced killer cell (CAR-CIK) technology featured at ASH
By Dr. Matthew Watson
DURHAM, N.C., Dec. 16, 2020 (GLOBE NEWSWIRE) -- CoImmune, Inc. today announced that its CAR-CIK technology was featured at the annual American Society of Hematology (ASH) meeting with an interim update on the phase 1/2 dose escalation clinical trial in B-cell acute lymphoblastic leukemia (B-ALL). The trial is being conducted at Ospedale San Gerardo, Monza, Italy by principal investigator Andrea Biondi, M.D. and at Papa Giovanni XXIII, Bergamo, Italy by principal investigator Alessandro Rambaldi, M.D. The presentation on was on December 7th during the immunotherapy session and was given by Dr. Chiara Magnani of the Tettamanti Research Center, Monza, Italy.
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Chimeric antigen receptor (CAR)-modified cytokine induced killer cell (CAR-CIK) technology featured at ASH
Tauriga Sciences Inc. Obtains its FEDLINKS Badge as a Verified Federal Government Vendor
By Dr. Matthew Watson
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Tauriga Sciences Inc. Obtains its FEDLINKS Badge as a Verified Federal Government Vendor
Tauriga Sciences Inc. to Resume the Clinical Development of its Proposed “Anti-Nausea” Pharmaceutical Grade Version of Tauri-Gum
By Dr. Matthew Watson
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Tauriga Sciences Inc. to Resume the Clinical Development of its Proposed “Anti-Nausea” Pharmaceutical Grade Version of Tauri-Gum
Bavarian Nordic Secures Second Part of Smallpox Vaccine Order from the U.S. Government
By Dr. Matthew Watson
COPENHAGEN, Denmark, December 16, 2020 – Bavarian Nordic A/S (OMX: BAVA, OTC: BVNRY) announced today that the U.S. Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response at the U.S. Department of Health and Human Services, has exercised an option covering the majority of the second year of performance under the USD $200 million order for JYNNEOS® (Smallpox and Monkeypox Vaccine, Live, Non-replicating) awarded in April 2020.
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Bavarian Nordic Secures Second Part of Smallpox Vaccine Order from the U.S. Government
AMAG Pharmaceuticals Files Submission in Response To the Food And Drug Administration’s Notice of Opportunity for a Hearing and Proposal To Withdraw…
By Dr. Matthew Watson
WALTHAM, Mass., Dec. 14, 2020 (GLOBE NEWSWIRE) -- AMAG Pharmaceuticals, Inc. has submitted its response to the FDA’s Notice of Opportunity for a Hearing (“NOOH”) regarding the Agency’s proposal to withdraw approval for Makena—also referred to as 17-OHPC—the only FDA-approved treatment, along with five generic versions, to reduce preterm birth in women with a singleton pregnancy who have a history of singleton spontaneous preterm birth.
CYBIN Closes Acquisition of Adelia Therapeutics; Bolsters Scientific Team and Grows IP Portfolio to 7 Patent Filings
By Dr. Matthew Watson
--Newly acquired novel psychedelic molecules diversify Cybin’s development portfolio, providing access to multiple future indications----Adelia brings a range of technologies related to novel therapeutics, delivery methods, and therapeutic regimens, along with six patent applications--
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CYBIN Closes Acquisition of Adelia Therapeutics; Bolsters Scientific Team and Grows IP Portfolio to 7 Patent Filings
AXIM® Biotechnologies to Present at the 13th Annual LD Micro Main Event Investor Conference on Monday, December 14
By Dr. Matthew Watson
SAN DIEGO, Dec. 14, 2020 (GLOBE NEWSWIRE) -- AXIM® Biotechnologies, Inc. (OTCQB: AXIM) (“AXIM® Biotech,” “AXIM” or “the Company”), an international healthcare solutions company targeting oncological and COVID-19 research, announced today that the Company’s CEO John W. Huemoeller II will be presenting at the 13th Annual LD Micro Main Event investor conference on Monday, December 14, 2020, at 11:00 a.m. PST/2:00 p.m. EST.
Eve & Co Completes Issuance of $550,000 Convertible Debentures
By Dr. Matthew Watson
STRATHROY, Ontario, Dec. 14, 2020 (GLOBE NEWSWIRE) -- Eve & Co Incorporated (“Eve & Co” or the “Company”) (TSX-V: EVE; OTCQX: EEVVF) is pleased to announce that it has successfully completed its non-brokered financing of unsecured convertible debentures in the principal amount of Cdn$550,000 (the “Debentures”) to certain individuals, including the Company’s Chief Executive Officer, Melinda Rombouts. The proceeds from the Debentures will be utilized for general working capital purposes.
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Eve & Co Completes Issuance of $550,000 Convertible Debentures
Adverum Biotechnologies Appoints Pharmaceutical Industry Veteran Dawn Svoronos to Board of Directors
By Dr. Matthew Watson
REDWOOD CITY, Calif., Dec. 14, 2020 (GLOBE NEWSWIRE) -- Adverum Biotechnologies, Inc. (Nasdaq: ADVM), a clinical-stage gene therapy company targeting unmet medical needs in ocular and rare diseases, today announced the appointment of Dawn Svoronos as an independent member of Adverum’s Board of Directors. Ms. Svoronos has three decades of global biopharmaceutical industry experience, spanning the United States, Canada, Europe, and Asia, gained during her 25-year career at Merck & Co.
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Adverum Biotechnologies Appoints Pharmaceutical Industry Veteran Dawn Svoronos to Board of Directors
Tauriga Sciences Inc. Surpasses the 10,000 Follower(s) Threshold on its Instagram Page – @taurigum
By Dr. Matthew Watson
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Tauriga Sciences Inc. Surpasses the 10,000 Follower(s) Threshold on its Instagram Page - @taurigum
Reviva Pharmaceuticals, Inc. and Tenzing Acquisition Corp. Complete their Business Combination and Trade as Reviva Pharmaceuticals Holdings, Inc.
By Dr. Matthew Watson
Combined Company to Trade on NASDAQ Post-closing under Tickers: RVPH and RVPHW
Aktana Hires Key Executives to Meet Escalating Demand for AI in Life Sciences
By Dr. Matthew Watson
Industry leaders bolster engineering, technology and professional services for Aktana’s growing customer roster Industry leaders bolster engineering, technology and professional services for Aktana’s growing customer roster
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Aktana Hires Key Executives to Meet Escalating Demand for AI in Life Sciences
Per Os Biosciences Expands Patent Portfolio for Chewing Gum Compositions Incorporating Cannabinoids
By Dr. Matthew Watson
Provides an efficient mechanism for delivering CBD to help treat all forms of pain Provides an efficient mechanism for delivering CBD to help treat all forms of pain
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Per Os Biosciences Expands Patent Portfolio for Chewing Gum Compositions Incorporating Cannabinoids
Bionexus Gene Lab Corp to Webcast Live at Life Sciences Investor Forum December 17th
By Dr. Matthew Watson
Company invites individual and institutional investors, as well as advisors and analysts, to attend real-time, interactive LifeSciencesInvestorForum.com Company invites individual and institutional investors, as well as advisors and analysts, to attend real-time, interactive LifeSciencesInvestorForum.com
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Bionexus Gene Lab Corp to Webcast Live at Life Sciences Investor Forum December 17th
Parexel Joins Decentralized Trials & Research Alliance (DTRA) to Enhance Patient Access, Increase Diversity and Accelerate Trial Timelines
By Dr. Matthew Watson
Company’s leading role in accelerating decentralized clinical trial adoption further reinforces its commitment to Patients-First approaches Company’s leading role in accelerating decentralized clinical trial adoption further reinforces its commitment to Patients-First approaches
Addex Announces Filing of Registration Statement for Proposed Public Offering of Securities
By Dr. Matthew Watson
Geneva, Switzerland, December 14, 2020 – Addex Therapeutics Ltd (SIX: ADXN and Nasdaq: ADXN), a clinical-stage pharmaceutical company pioneering allosteric modulation-based drug discovery and development announced today that it has filed a registration statement with the U.S. Securities and Exchange Commission (SEC) for a proposed underwritten public offering of shares, including those to be settled in the form of American Depositary Shares (ADSs). Each ADS represents the right to receive six shares of Addex. The terms of the offering have not been determined, and the offering is subject to market and other conditions, and there can be no assurance as to whether or when the offering may be completed. The Company will be concurrently offering the shares in Europe (other than Switzerland) in a private placement to qualified investors, and in Switzerland through private placements.
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Addex Announces Filing of Registration Statement for Proposed Public Offering of Securities