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FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA

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Dec 18

ABBOTT STRENGTHENS STRUCTURAL HEART PORTFOLIO WITH NEW CLIP DELIVERY SYSTEM

Abbott has launched its clip delivery system, a minimally invasive heart valve repair device to treat mitral regurgitation in India. ...
Dec 18

Vir Biotechnology and GSK announce start of NIH-sponsored ACTIV-3 trial evaluating VIR-7831 in hospitalized adults with COVID-19

ACTIV-3 is an NIH-led public-private partnership designed to accelerate the development of the most promising treatments and vaccine candidates for COVID-19....
Dec 18

NATCO launches anti blood clot tablet Rivaroxaban in India

Rivaroxaban is currently sold by Bayer under the brand name of Xarelto, in the Indian market....
Dec 18

FDA approves GSK’s BENLYSTA as the first medicine for adult patients with active lupus nephritis in the US

BENLYSTA is the first medicine approved to treat systemic lupus and adults with active lupus nephritis, an important treatment advance for patients with this incurable ...
Dec 18

Biocon Biologics signs an MoU with CSSC in Tanzania for Mission 10 cents

Tanzania will be the first country in Africa that will benefit from this collaboration between Biocon Biologics and CSSC....
Dec 17

FDA Grants Priority Review to Merck’s Supplemental Biologics License Application for KEYTRUDA

Patients with newly diagnosed esophageal and GEJ cancer face an aggressive disease with a poor prognosis, despite the currently available treatment options...
Dec 17

Cipla Launches ‘CIPtest’ Rapid Antigen Detection Test for COVID-19 Diagnosis

CIPtest is a reliable high-performing kit that has been validated and approved by ICMR....
Dec 16

KEYTRUDA Plus LENVIMA Combination Demonstrated Statistically Significant Improvement in Overall Survival

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Dec 16

Imfinzi recommended for approval in the EU by CHMP for non-small cell lung cancer

This new dosing option is consistent with the approved Imfinzi dosing in extensive-stage small cell lung cancer and once approved, will be available to ...
Dec 15

Sanofi renews partnership with the WHO to fight Neglected Tropical Diseases

Sanofi renewed a partnership agreement with the WHO, consolidating a 20-year collaboration to fight some of the most Neglected Tropical Diseases...
Dec 15

Trastuzumab deruxtecan recommended for approval in the EU by CHMP for HER2-positive metastatic breast cancer

The impact of the disease is significant, with breast cancer responsible for more than 137,000 deaths per year....
Dec 14

Trixeo Aerosphere approved in the EU for maintenance treatment of COPD

COPD is a progressive disease, which can cause obstruction of airflow in the lungs resulting in debilitating bouts of breathlessness and is the third leading ...
Dec 14

Biocon Biologics, Mylan get CHMP recommendation for approval of biosimilar insulin Aspart

Biocon subsidiary Mylan advances their ...
Dec 14

Bristol Myers Squibb Receives Positive CHMP Opinion for Inrebic for Adult Patients with Myelofibrosis

If approved, Inrebic will become the first new therapy for myelofibrosis in Europe in nearly a decade....
Dec 11

Bristol Myers Squibb Announces Settlement of U.S. Patent Litigation for REVLIMID with Cipla

Bristol Myers Squibb today announced that its wholly-owned subsidiary, Celgene, and Cipla have settled their litigation related to patents for REVLIMID....
Dec 11

Alembic Pharmaceuticals announces USFDA Final Approval for Asenapine Sublingual Tablets

Asenapine is an atypical antipsychotic indicated for bipolar I disorder as adjunctive treatment to lithium or valproate in adults....
Dec 11

Merck Receives Positive EU CHMP Opinion for KEYTRUDA as First-Line Treatment for Metastatic Microsatellite Instability

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Dec 11

ViiV Healthcare announces positive CHMP opinion for Rukobia, for the treatment of adults with multidrug-resistant HIV

Fostemsavir addresses a critical unmet need in HIV care for those with little to no treatment options left....
Dec 11

Enhertu continues to demonstrate durable responses with new data from DESTINY-Breast01 in HER2

Enhertu continued to demonstrate impressive efficacy and durable responses in patients with HER2-positive metastatic breast cancer following two or more prior HER2-based regimens....
Dec 10

Glenmark Pharmaceuticals receives ANDA tentative approval for Axitinib Tablets

According to IQVIA sales data for the 12 month period ending October 2020, the Inlyta Tablets market achieved annual sales of approximately $518.8 million*....
Dec 01

Crestor to be divested to Grünenthal in Europe

AstraZeneca has agreed to sell the rights to Crestor and associated medicines in over 30 countries in Europe, except the UK and Spain....
Dec 01

Eisai receives approval for indication expansion of anti-epileptic agent fycompa for use in pediatric patients

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Dec 01

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