NeuroThera and Clearmind Advance MDMA-PEA Program With U.S. Patent Application Publication

SciSparc Ltd.(“Company” or “SciSparc”), announced that its  subsidiary, NeuroThera Labs Inc. (TSXV: NTLX) ("NeuroThera"), a ...

August 26, 2026 | Wednesday | News
FDA Grants Orphan Drug Designation to Lakefront’s Gamgertamig for Pemphigus

Lakefront Biotherapeutics NV  announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation to gamgertamig for the ...

August 26, 2026 | Wednesday | News
Leads Biolabs Advances Opamtistomig into Expansion Phase in First-Line Esophageal Cancer Trial

Nanjing Leads Biolabs Co., Ltd. (“Leads Biolabs” or the “Company,”  announced that Opamtistomig (LBL-024), the Company&rsquo...

August 26, 2026 | Wednesday | News
Ipsen Completes Acquisition of Kartos Therapeutics, Adding Phase III Myelofibrosis Drug Candidate

Ipsen announced it has completed the acquisition of Kartos Therapeutics, a clinical-stage biopharmaceutical company adding late-stage MDM2 inhibitor navt...

August 24, 2026 | Monday | News
Johnson & Johnson Wins EU Approval for TECVAYLI Plus Daratumumab in Earlier-Line Multiple Myeloma

Johnson & Johnson announced that the European Commission (EC) has approved an indication extension for TECVAYLI®(teclistamab) in combination with...

August 24, 2026 | Monday | News
Milestone Pharmaceuticals Enrolls First Patient in Phase 3 Trial of Etripamil for AFib-RVR

Milestone® Pharmaceuticals Inc. , a biopharmaceutical company focused on the development and commercialization of innovative cardiovascular medi...

August 24, 2026 | Monday | News
Orum Therapeutics Wins FDA Clearance for ORM-1153 AML Degrader-Antibody Conjugate

Orum Therapeutics(“Orum” or the “Company”), a biotechnology company pioneering the field of degrader-antibody conjugates (DACs), ...

August 24, 2026 | Monday | News
Teva’s Ecopipam NDA Accepted by FDA for Pediatric Tourette Syndrome

Ecopipam (EBS-101) is a first-in-class selective D1 (dopamine) receptor antagonist with Orphan Drug designation NDA acceptance is supported by po...

August 21, 2026 | Friday | News
ACTG Opens STAIR-HIV Trial to Evaluate Alendronate as an HIV Latency-Reversing Agent

ACTG, a global clinical trials network focused on HIV and other infectious diseases, announced the opening of STAIR-HIV (Small Trial of Alendronate Impac...

August 21, 2026 | Friday | News
Syneos Health Advances Enterprise AI Ecosystem for Clinical Development

Syneos Health®, a leading fully integrated biopharmaceutical solutions organization, announced the continued advancement of its AI ecosystem – ...

August 20, 2026 | Thursday | Opinion
Radiopharm Theranostics Schedules FDA Meeting for RAD101 Phase 3 Trial

RAD 101 Phase 2b trial demonstrated 93% concordance with MRI across all evaluable lesions, meeting the Phase 2 trial's primary endpoint End-of-Phase 2 m...

August 19, 2026 | Wednesday | News
Pfizer and Valneva Lyme Disease Vaccine Application Validated by EMA

Pfizer Inc. (NYSE: PFE) and Valneva SE (Nasdaq: VALN; Euronext Paris: VLA)  announced that the European Medicines Agency (EMA) has validated the Mar...

August 18, 2026 | Tuesday | News
Enigma Biomedical USA Receives FDA Approval for TAUKLARIFY Tau PET Imaging Agent

-Enigma Biomedical USA (EB USA) today announced the U.S. Food and Drug Administration (FDA) approval of TAUKLARIFY™ (florquinitau F 18 injection, a...

August 18, 2026 | Tuesday | News
Nanochon Receives Panama Approval to Begin First-in-Human Chondrograft Knee Study

Nanochon, a medical device company developing Chondrograft, a novel patented implant for the treatment of articular cartilage defects of the knee, announ...

August 17, 2026 | Monday | News

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