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Dr Reddy’s buys select anti-allergy brands from Glenmark in Russia and other CIS countries

Glenmark to launch Ryaltris, their global anti-allergy brand, in Russia and other CIS countries after the divestment ...
Nov 30

Dupixent approved by European Commission as first and only biologic medicine for children aged 6 to 11 years with severe atopic dermatitis

Atopic dermatitis is a chronic inflammatory disease of the skin that can be debilitating, and severe disease can significantly impact many aspects of life for ...
Nov 30

Hon'ble Prime Minister of India, Shri Narendra Modiji's inspiring presence at the Zydus Biotech Park

Hon'ble Prime Minister's leadership vision, in-depth understanding and knowledge of the facts guided us in facilitating the interactions and discussions on the ...
Nov 30

Roche announces FDA approval of Xofluza

Xofluza for the prevention of influenza following contact with an infected person...
Nov 27

Apollo Hospitals, Bangalore has introduced Robotic Assisted Joint Replacement Program

The Robotic system has an advanced computed program that relays precise information about the knee with 3D mapping....
Nov 27

RhoVac's Prostate Cancer Drug Candidate, RV001, is granted Fast Track Designation by the FDA

Latest FDA News Nov 26, 2020...
Nov 26

Glenmark Pharmaceuticals secures its position in the prestigious Dow Jones Sustainability Emerging Markets Index

DJSI is one of the world’s most respected and widely accepted sustainability benchmarks globally with only the top-ranked companies in terms of Corporate ...
Nov 26

Laurus Labs forays into biotech, acquires majority stake in Richcore Lifesciences

Laurus Labs to acquire 72.55 per cent of Richcore’s shares for a value of Rs 246.7 crores...
Nov 26

Piramal Sarvajal and Center for Water and Sanitation Launch Composite Water Vulnerability Index Tool

Piramal Sarvajal, the safe drinking water initiative of Piramal Foundation launched a tool named Composite Water Vulnerability Index at its recent Webinar on ‘Sustainable Water ...
Nov 25

Bristol Myers Squibb Receives European Commission Approval for Opdivo

Bristol Myers Squibb announced the approval of Opdivo for the treatment of adults with unresectable advanced, recurrent or metastatic esophageal squamous cell carcinoma ...
Nov 25

Alembic Pharmaceuticals announces its joint venture Aleor Dermaceuticals receives USFDA Tentative Approval for Testosterone Gel

Testosterone Gel, is indicated for replacement therapy in adult males for conditions associated with a deficiency or absence of endogenous testosterone....
Nov 25

Lokelma label update approved in China for patients with hyperkalaemia on chronic haemodialysis

The NMPA has approved a dosing label update in China for AstraZeneca’s Lokelma to include patients with hyperkalaemia on chronic haemodialysis....
Nov 25

Lupin launches Tacrolimus Capsules USP

Tacrolimus Capsules are the generic equivalent of Prograf Capsules of Astellas Pharma US, Inc. and are indicated for the prophylaxis of organ rejection....
Nov 25

Acquisition adds to Merck’s suite of clinical programs in response to SARS-CoV-2/COVID-19

Meaningful new therapeutic options are desperately needed for possibly millions of people around the world who will develop severe or critical COVID-19 disease...
Nov 23

AZD1222 vaccine met primary efficacy endpoint in preventing COVID-19

Positive high-level results from an interim analysis of clinical trials of AZD1222 in the UK and Brazil showed the vaccine was highly effective in ...
Nov 23

GSK starts phase 3 study of RSV maternal candidate vaccine

Currently no vaccine is available for respiratory syncytial virus...
Nov 23

Recently published data on Favipiravir as treatment for mild to moderate COVID-19 demonstrates significant improvement in time to clinical cure

The oral antiviral medication Favipiravir, which prevents the replication phase of the virus life-cycle, leads to significant improvement in clinical cure in patients with ...
Nov 23

PFIZER DOSES FIRST PARTICIPANT IN PHASE 3 STUDY EVALUATING ANTI-TFPI INVESTIGATIONAL THERAPY

An anti-tissue factor pathway inhibitor being evaluated for the treatment of people with severe hemophilia A or B, with or without inhibitors....
Nov 23

Merck Submits Applications for Licensure of V114, the Company’s Investigational 15-valent Pneumococcal Conjugate Vaccine

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Nov 23

Strides receives USFDA approval for Prednisone Tablets

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Nov 23

European Commission approves MenQuadfi, the latest innovation in meningococcal vaccination

The EC has approved MenQuadfi for active immunization against invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, W and Y....
Nov 23

GSK and MMV present positive data on treatment for Plasmodium vivax malaria in children

GSK and MMV today presented positive data from the TEACH study of tafenoquine, an 8-aminoquinoline, for the prevention of relapse of Plasmodium vivax malaria ...
Nov 20

RESULTS FROM PHASE 3 CROWN TRIAL OF PFIZER’S LORBRENA IN PREVIOUSLY UNTREATED ALK-POSITIVE LUNG CANCER PUBLISHED IN THE NEW ENGLAND JOURNAL OF MEDICINE

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Nov 19

Catalent acquires Bone Therapeutic's cell therapy manufacturing subsidiary SCTS

Under the terms of the transaction, Catalent acquires Bone Therapeutics’ cell therapy manufacturing subsidiary, SCTS, for gross proceeds of €12 million...
Nov 18

ABBOTT STRENGTHENS STRUCTURAL HEART PORTFOLIO WITH NEW CLIP DELIVERY SYSTEM FOR NON-INVASIVE TREATMENT OF LEAKY MITRAL VALVES

Clinical evidence for this device demonstrates safety and efficacy for people suffering from mitral regurgitation...
Nov 18

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