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BioSpace News Archive
Browse BioSpace’s published news and press releases by year, month, and day.
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Lone Star Bio
LivaNova to Present at the Piper Sandler Healthcare Conference
LivaNova PLC, a market-leading medical technology company, announced Bill Kozy, Interim Chief Executive Officer and Board Chair of LivaNova, will present in a fireside chat at the Piper Sandler Healthcare Conference in New York.
November 9, 2023
·
2 min read
Biotech Beach
Masimo to Present in 2023 Jefferies London Healthcare Conference
Masimo announced that its management will participate in the Jefferies London Healthcare Conference on Wednesday, November 15, 2023 at 3:00 pm GMT.
November 9, 2023
·
3 min read
Policy
U.S. Food and Drug Administration Accepts for Priority Review Bristol Myers Squibb’s Application for Breyanzi (lisocabtagene maraleucel) for Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL)
Bristol Myers Squibb announced that the U.S. Food and Drug Administration has accepted the supplemental Biologics License Application for Breyanzi to expand its current indication to include the treatment of adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma who received a prior Bruton tyrosine kinase inhibitor and B-cell lymphoma 2 inhibitor.
November 9, 2023
·
18 min read
Vetter’s European Clinical Site Receives Permanent Manufacturer’s Authorization
Vetter, a leading global Contract Development and Manufacturing Organization (CDMO), has received the permanent Manufacturer’s Authorization for its clinical development site in Rankweil, Austria.
November 9, 2023
·
3 min read
Drug Development
Alladapt Immunotherapeutics Presents Phase 1/2 Harmony Data Demonstrating Therapeutic Potential and Safety of ADP101 for the Treatment of Food Allergy at 2023 ACAAI Annual Meeting
Alladapt Immunotherapeutics, Inc. announced that data from the Phase 1/2 Harmony study will be presented at the 2023 Annual Scientific Meeting of the American College of Asthma, Allergy and Immunology taking place Nov. 9-13.
November 9, 2023
·
7 min read
Drug Development
SOLA Biosciences Presents Preclinical Proof-of-Concept Data for SOL-257, a Gene Therapy Targeting Misfolded TDP-43 in ALS, at Neuroscience 2023 and ALS One Symposium
As a pioneer in innovative chaperone technology, SOLA Biosciences Inc. will present its compelling preclinical proof-of-concept data for SOL-257, a targeted gene therapy for misfolded TDP-43 in Amyotrophic Lateral Sclerosis, at Neuroscience 2023 in Washington, D.C. on November 15 and the ALS One Symposium on November 17.
November 9, 2023
·
2 min read
PharmaDrug Inc. Announces Grant of Stock Options
PharmaDrug Inc. (CSE: PHRX) (OTC Pink: LMLLD) (“PharmaDrug” or the “Company”), announces that it has granted a total of 6,250,000 stock options (“Options”) to purchase common shares of the Company to certain officers,
November 9, 2023
·
4 min read
Kiora Pharmaceuticals Reports Q3 2023 Results; Expanding Clinical Development of KIO-301 for Inherited Retinal Diseases Based on Encouraging Results of ABACUS-1 Study in Retinitis Pigmentosa
Kiora Pharmaceuticals, Inc. (NASDAQ: KPRX) (“Kiora” or the “Company”) today announced its third quarter 2023 financial results and is providing an update on its plans to advance clinical development of KIO-301 for other inherited retinal diseases.
November 9, 2023
·
7 min read
Business
Cell MedX Corp. Appoints Audit Committee and Accepts Resignation of Chief Operating Officer
Cell MedX Corp. (OTC Pink: CMXC) (“Cell MedX” or the “Company”), a biotech company focusing on the discovery, development and commercialization of therapeutic and non-therapeutic products that promote general wellness,
November 9, 2023
·
3 min read
Drug Development
Entera Bio Reports Key Milestone Relating to Oral PTH (1-34) Peptide (EB613) Phase 3 Program: ASBMR-SABRE Has Submitted to FDA the Full Qualification Plan to Approve BMD as a Surrogate Endpoint for Osteoporosis
Entera Bio Ltd. reports that the American Society for Bone and Mineral Research has announced that the SABRE project team has submitted to the U.S. Food and Drug Administration its full qualification plan to use the treatment-related change in bone mineral density as a surrogate endpoint for fractures in future trials of new anti-osteoporosis drugs.
November 9, 2023
·
8 min read
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