Takeda's LIVTENCITY® Approved in China for Post-Transplant CMV Treatment

Approval Based on Phase 3 TAK-620-303 SOLSTICE Study Demonstrating Maribavir Was Superior to Conventional Therapies at Week 8, for Primary Endpoint1-...

December 22, 2023 | Friday | News
Inventiva Enrolls First Patient in China for NATiV3 Trial and Updates Clinical Development Program

The first patient was randomized in China in the NATiV3 Phase III clinical trial, triggering a milestone payment of $3 million from CTTQ to Inventiva.&nb...

December 21, 2023 | Thursday | News
Sanofi Ends Tusamitamab Ravtansine Program Due to Phase 3 Trial Setback in 2L NSCLC

CARMEN-LC03 trial did not meet dual primary endpoint of improving progression-free survival; tusamitamab ravtansine clinical development program will be ...

December 21, 2023 | Thursday | News
ImpriMed Secures $23M in Series A to Expand AI-Powered Cancer Treatment Technology

ImpriMed, a leading precision medicine startup focused on leveraging artificial intelligence to improve cancer treatment,  announced the close of a $2...

December 20, 2023 | Wednesday | News
Piramal Pharma Solutions Inaugurates ADC Manufacturing Expansion in Grangemouth, Scotland

Ribbon cutting and commissioning of a multipurpose state-of-the-art Antibody-Drug Conjugate (ADC) manufacturing facility that expands capacity by approxi...

December 19, 2023 | Tuesday | News
FDA Approves PADCEV® with KEYTRUDA® for Advanced Bladder Cancer

– PADCEV plus pembrolizumab approved based on groundbreaking EV-302 trial – – Confirmatory trial found PADCEV plus pembrolizumab nearly ...

December 18, 2023 | Monday | News
First patient in China has been dosed in the YOLT-201 clinical trial for the treatment of Hereditary ATTR-CM

The study by YolTech is a single-arm, open-label, dose-escalation clinical trial (Clinicaltrials.gov: NCT06082050). This trial's primary objectives are to ...

December 18, 2023 | Monday | News
CHMP Greenlights Biogen's SKYCLARYS® for Rare Neurodegenerative Disease

Friedreich’s ataxia is a genetic, debilitating and life-shortening neuromuscular disease1 Milestone highlights Biogen’s growing portfolio in...

December 18, 2023 | Monday | News
Teva and Biolojic Design Ink Exclusive License for Atopic Dermatitis and Asthma Antibody Therapy

Biolojic’s BD9 is a multibody that was computationally designed as a multi specific antibody targeting IL-13 / TSLP to treat inflammatory diseases....

December 15, 2023 | Friday | News
Innovent Secures New Reimbursement Milestones for TYVYT® and BYVASDA® in China

In the updated NDRL, TYVYT® expands its coverage to the seventh new indication for the treatment of patients with epidermal growth factor receptor (EGF...

December 13, 2023 | Wednesday | News
Bristol Myers Squibb's Opdivo and Yervoy Combo Shows Positive Results in Phase 3 Trial for Metastatic Colorectal Cancer

Opdivo (nivolumab) plus Yervoy (ipilimumab) demonstrates statistically significant and clinically meaningful improvement in progression-free survival compa...

December 08, 2023 | Friday | News
IMIDomics and Bristol Myers Squibb Extend Partnership for Inflammatory Disease Research

In 2016, IMIDomics entered into a strategic partnership with BMS to harness their unique clinical and molecular database, and multidimensional analysis con...

December 07, 2023 | Thursday | News
Cyprium Transfers CUTX-101 for Menkes Disease to Sentynl, a Zydus Lifesciences Subsidiary

Cyprium received $4.5 million payment upon closing and remains eligible to receive royalties and up to $129 million in aggregate development and sales mile...

December 07, 2023 | Thursday | News
Novartis' Fabhalta® (iptacopan) gains FDA approval as the first oral monotherapy for adults with PNH, showing superior hemoglobin improvement without transfusions.

Approval based on APPLY-PNH trial in adults with PNH and anemia despite prior anti-C5 treatment, and supported by the APPOINT-PNH study in complement inh...

December 06, 2023 | Wednesday | News

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