Innovent Biologics Receives NMPA Approval for DOVBLERON® (Taletrectinib Adipate) as a Treatment for ROS1-Positive NSCLC

Innovent Biologics, Inc. ("Innovent") (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high quality me...

January 03, 2025 | Friday | News
Hanx Biopharmaceuticals Doses First Patient in Australia for Phase 1 Clinical Trial of Groundbreaking Cancer Therapy HX044

Hanx Biopharmaceuticals, CO. Ltd, an innovative biotechnology company developing next-generation immunotherapies to address the challenges of unmet medical...

January 03, 2025 | Friday | News
Qualia NAD+ Achieves Clinical Proof for Boosting NAD+ Levels by 67% through Simple Supplementation

 Qualia NAD+, a new supplement by the pioneering Qualia Life Sciences team has now achieved clinical proof that it can boost NAD+ levels through simpl...

January 03, 2025 | Friday | News
SciSparc Secures Renewal to Advance SCI-210 Clinical Trial for Autism Spectrum Disorder

SciSparc, a specialty clinical-stage pharmaceutical company focusing on the development of therapies to treat disorders of the central nervous system, to...

January 02, 2025 | Thursday | News
CARsgen Therapeutics Launches Investigator-Initiated Trial in China for KJ-C2219, an Allogeneic CAR T-Cell Therapy Targeting CD19/CD20

CARsgen Therapeutics Holdings Limited (Stock Code: 2171.HK), a company focused on innovative CAR T-cell therapies for the treatment of hematologic malignan...

January 01, 2025 | Wednesday | News
BeiGene Exercises Option for DB1312/BG-C9074, Securing Global Rights to DualityBio's B7H4 Antibody-Drug Conjugate

Duality Biologics ("DualityBio") announced that, BeiGene. Ltd. has exercised its exclusive option for the B7H4 antibody-drug conjugate (ADC) DB1312/BG-C907...

December 31, 2024 | Tuesday | News
ADC Therapeutics Completes Enrollment in Phase 3 LOTIS-5 Trial of ZYNLONTA® (Loncastuximab Tesirine) for Relapsed or Refractory DLBCL

ADC Therapeutics SA (NYSE: ADCT), a commercial-stage global leader and pioneer in the field of antibody drug conjugates (ADCs),  announced the co...

December 31, 2024 | Tuesday | News
VYVDURA® (efgartigimod alfa and hyaluronidase-qvfc) Approved by Japan’s MHLW for Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Halozyme Therapeutics, Inc. (NASDAQ: HALO) (Halozyme) announced that argenx's VYVDURA (efgartigimod alfa and hyaluronidase-qvfc), which is co-formulated wi...

December 31, 2024 | Tuesday | News
Takeda Receives Japanese Regulatory Approval for HYQVIA® in Primary and Secondary Immunodeficiency Disorders

Halozyme Therapeutics, Inc. (NASDAQ: HALO) (Halozyme) announced that Takeda received regulatory approval for HYQVIA® [Immune Globulin Infusion 10%...

December 31, 2024 | Tuesday | News
Sangamo Therapeutics Regains Rights to Giroctocogene Fitelparvovec Following Pfizer's Decision to End Collaboration

Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, announced it will regain development and commercialization rights to giroctocog...

December 31, 2024 | Tuesday | News
Novartis Announces Positive Phase III STEER Study Results for OAV101 IT in Spinal Muscular Atrophy Type 2 Patients

Novartis announced positive topline results from the Phase III STEER study. This pivotal study assessed the efficacy and safety of investigational intrathe...

December 31, 2024 | Tuesday | News
Novartis Reports Positive Phase III STEER Trial Results for SMA Gene Therapy

The Phase III STEER study met its primary endpoint showing an increase from baseline in HFMSE total score in patients with SMA treated with intrathecal...

December 30, 2024 | Monday | News
Johnson & Johnson Secures EC Approval for Amivantamab-Lazertinib Combo as First-Line Treatment for EGFR-Mutated NSCLC

  Janssen-Cilag International NV, a Johnson & Johnson company,  announced the European Commission (EC) approval of RYBREVANT®▼ (amivan...

December 30, 2024 | Monday | News
BMS Gains FDA Approval for Opdivo Qvantig, First Subcutaneous PD-1 Inhibitor with Three-Minute Administration

-Bristol Myers Squibb (NYSE: BMY)  announced that the U.S. Food and Drug Administration (FDA) granted approval for Opdivo Qvantig™&nbs...

December 30, 2024 | Monday | News

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