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	Forxiga recommended for approval in the EU by CHMP for heart failure If approved, Forxiga would become the first SGLT2 inhibitor indicated for heart failure with reduced ejection fraction in patients with and without type-2 diabetes... Oct 19
	Zydus Cadila receives tentative approval for Tofacitinib Extended-Release Tablets Zydus Cadila has received tentative approval to market 11 mg Tofacitinib Extended-Release Tablets... Oct 19
	Recommendation of triple-combination therapy based on positive results from ETHOS and KRONOS Phase III trials Trixeo Aerosphere recommended for approval in the EU by CHMP for the maintenance treatment of COPD... Oct 19
	Glenmark Pharmaceuticals receives ANDA approval for Sirolimus Tablets, 0.5 mg, 1 mg and 2 mg Glenmark received approval from ANDA for Sirolimus Tablets, a generic version of Rapamune Tablets... Oct 19
	CHMP recommends approval of Dupixent for children aged 6 to 11 years with severe atopic dermatitis Dupixent combined with TCS in children aged 6 to 11 years with severe atopic dermatitis that is uncontrolled on topical prescription therapies... Oct 16
	ViiV Healthcare receives positive CHMP opinion for long-acting regimen for the treatment of HIV ViiV Healthcare announced CHMP issed positive opinion recommending Vocabria in combination with Rekambys and Edurant for the treatment of HIV-1 ... Oct 16
	FDA Approves Expanded Indication for Merck’s KEYTRUDA in Adult Patients With classical Hodgkin Lymphoma (cHL) ... Oct 15
	Sanofi and Translate Bio mRNA COVID-19 vaccine candidate induced high antibody levels in preclinical studies Sanofi and Translate Bio today announced the preclinical results of an mRNA-based vaccine candidate against SARS-CoV-2... Oct 15
	Glenmark introduces a generic version of NINDANIB for the treatment of Pulmonary Fibrosis Glenmark being a leader in the area of respiratory has been amongst the first to launch the branded generic version for the treatment of Pulmonary ... Oct 14
	Dupixent reduced severe asthma attacks in children and is the only biologic to demonstrate improvement in children’s lung function A pivotal Phase 3 trial of Dupixent met its primary and all key secondary endpoints in children aged 6 to 11 years with uncontrolled moderate-... Oct 13
	Rhizen Pharmaceuticals S.A. and Curon Biopharmaceutical Limited Announce an Exclusive License Agreement to Develop and Commercialize Tenalisib Rhizen and Curon's exclusive license agreement for Tenalisib, a dual PI3K delta & gamma inhibitor in the Greater China region.... Oct 12
	Rhizen Pharmaceuticals S.A. and Curon Biopharmaceutical Limited Announce an Exclusive License Agreement to Develop and Commercialize Tenalisib Rhizen and Curon's exclusive license agreement for Tenalisib, a dual PI3K delta & gamma inhibitor in the Greater China region.... Oct 12
	Dr. Reddy's Laboratories announces the launch of Cinacalcet Tablets in the U.S. Market Dr. Reddy’s Laboratories Ltd., today announced the launch of Cinacalcet Tablets, a generic version of Sensipar Tablets, approved by the USFDA... Oct 01
	PFIZER RECEIVES FDA FAST TRACK DESIGNATION FOR DUCHENNE MUSCULAR DYSTROPHY Pfizer Inc. today announced that its investigational gene therapy candidate being developed to treat Duchenne muscular dystrophy ... Oct 01
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