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You searched for : LatestPharmaNewsOct2  

Reddy's partners with Department of Biotechnology for Sputnik V vaccine clinical trials in India

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Oct 29

Dupixent reports safe administrations for young patients with moderate-to-severe atopic dermatitis

These data reinforce the well-established long-term safety profile of Dupixent in moderate-to-severe atopic dermatitis....
Oct 29

Cipla launches ‘ELIFast’ for COVID-19 antibody detection

Cipla will be responsible for the marketing and distribution of the SARS CoV-2-IgG antibody detection ELISA that will be manufactured by KARWA Ltd....
Oct 28

Piramal Pharma Consumer Products Division’s Tri-Activ Disinfectant Spray For Multi-Surfaces is 99.9% Effective Against the Covid-19 Virus in 1 Minute

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Oct 27

FDA GRANTS PRIORITY REVIEW AND EMA ACCEPTS REGULATORY SUBMISSION FOR PFIZER’S ABROCITINIB FOR PATIENTS WITH ATOPIC DERMATITIS

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Oct 27

Dupixent late-breaking pivotal data showing significant improvement in eosinophilic esophagitis signs and symptoms

New late-breaking data showing additional improvements in disease severity and extent at the microscopic level ...
Oct 26

Decreases in Americans' Primary Care Visits May Lead to Late Diagnoses of Potentially Serious Conditions

The Bristol Myers Squibb–Pfizer Alliance, with the support of leading advocacy organizations and medical societies, announces the launch of the No Time to Wait ...
Oct 26

FDA authorises restart of the COVID-19 AZD1222 vaccine US Phase III trial

Clinical trials for the AstraZeneca Oxford coronavirus vaccine, AZD1222, have resumed across the world...
Oct 24

Lupin Wins Five INDIASTAR 2020 Awards for Excellence in Packaging

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Oct 23

Zydus Cadila receives final approval from USFDA for Albuterol Tablets

Albuterol is a bronchodilator and it helps open up the airways in your lungs to make it easier to breathe. ...
Oct 23

Alembic Pharmaceuticals announces its joint venture Aleor Dermaceuticals receives USFDA Final Approval for Tavaborole Topical Solution

The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Topical Solution, 5%, of Anacor Pharmaceuticals, Inc....
Oct 22

Alembic Pharmaceuticals announces USFDA Final Approval for Fenofibrate Capsules USP, 67 mg, 134 mg and 200 mg.

Fenofibrate Capsules USP, 67 mg, 134 mg and 200 mg have an estimated market size of US$ 17 million for twelve months ending June 2020 ...
Oct 21

Merck Announces Positive Topline Results from Two Additional Phase 3 Adult Studies Evaluating V114, Merck’s Investigational 15-valent Pneumococcal Conjugate Vaccine

Pneumococcal disease in adults is on the rise globally, in part driven by disease-causing serotypes not targeted by the currently available pneumococcal conjugate vaccine...
Oct 21

Zydus Cadila receives Final Approval from USFDA for Solifenacin Succinate Tablets

Zydus Cadila has received final approval from the USFDA to market Solifenacin Succinate Tablets, in the strengths of 5 mg and 10 mg...
Oct 21

Cipla launches Nintib to treat Idiopathic Pulmonary Fibrosis, in continuation of its fight against rare lung diseases

Cipla Limited today announced that it has launched generic Nintedanib for the treatment of Idiopathic Pulmonary Fibrosis ...
Oct 21

No significant clinical benefit with Umifenovir addition in COVID-19 treatment: Glenmark clinical study

Umifenovir did not show superior clinical outcomes when added to Favipiravir treatment. The trial did not meet key end-points ...
Oct 21

ViiV healthcare development program on cabotegravir and rilivirine has no pandemic interruptions

ViiV Healthcare, today announced the positive findings of a pooled analysis of COVID-19-related impacts across the investigational long-acting cabotegravir and rilpivirine clinical ...
Oct 21

Dr. Reddy’s announces the re-launch of OTC Famotidine Tablets USP, store-brand equivalent of Pepcid AC in the U.S. Market

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Oct 20

USFDA Accepts for Priority Review Applications for OPDIVO in Combination with CABOMETYX in Advanced Renal Cell Carcinoma

Results from CheckMate -9ER recently presented during a Presidential Symposium at the European Society for Medical Oncology Virtual Congress...
Oct 19

EMA accepts regulatory submission for avalglucosidase alfa for Pompe disease

Avalglucosidase alfa is an investigational enzyme replacement therapy, which, if approved, would offer a potential new standard of care for patients with Pompe disease...
Oct 02

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