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	Clinical Interventions in Chronic Hepatitis B and C: Antiviral Efficacy, Liver Fibrosis Scoring, and Monitoring Effective management of chronic hepatitis B and C requires timely antiviral therapy, accurate liver fibrosis assessment, and structured long-term monitoring. Advances in direct-acting ... Aug 11
	Interventions in Facial Nerve Pathology: Bell’s Palsy & Ramsay Hunt Peripheral facial nerve paralysis is an acute neuro-otological condition that demands prompt diagnosis and timely intervention to preserve facial nerve function and improve recovery ... Jul 11
	HTD1801, a First-in-Class Anti-inflammatory Metabolic Modulator, Demonstrates Durable 52-Week Efficacy and Safety in Two Phase III Trials in Type 2 Diabetes Mellitus These 52-week data reinforce HTD1801's potential as a truly differentiated therapeutic to concurrently address metabolic dysregulation, inflammation, and renal progression in type 2 ... Oct 31
	The Twin Therapy that Could Help Win India’s Fight Against Diabetes As India continues its journey towards becoming the diabetes capital of the world, the medical fraternity faces the challenge of changing old habits both in ... Oct 08
	Berberine Ursodeoxycholate (HTD1801) Consistently Demonstrates Comprehensive Benefits for Patients with Type 2 Diabetes Mellitus, Approaching NDA ... Apr 15
	Lilly Launches Mounjaro® (tirzepatide), offering a new option for the treatment of obesity and type 2 diabetes ... Mar 20
	EASD 2024 | HighTide Therapeutics Presents Oral Reports of Phase 2 Studies Highlighting Benefits of Berberine Ursodeoxycholate (HTD1801).... Sep 11
	European Commission approves Teysuno in metastatic colorectal cancer Latest Corporate news updates; Pharma Feb 3rd 2022... Feb 03
	Innovent and GenFleet announce Exclusive Global License agreement for GFH925 (KRAS G12C Inhibitor) Latest Pharma News update... Sep 03
	ImmixBio and BeiGene to evaluate combination of IMX-110 and Tislelizumab in solid tumors Latest Pharma News Update... Aug 31
	Adagene Announces the Third Clinical Trial Collaboration with Merck to Advance Anti-CD137 Agonist, ADG106 Latest Pharma Update... Aug 23
	Alkermes Receives FDA fast track designation for Nemvaleukin Alfa for the treatment of Mucosal Melanoma FDA News Update... Aug 05
	Bristol Myers Squibb Provides Update on CheckMate -651 Trial Evaluating Opdivo Plus Yervoy Versus EXTREME Regimen as First-Line Treatment for Squamous Cell Carcinoma ... Jul 17
	Immutep receives FDA and IRB approval in the US for Phase IIb TACTI-003 trial in HNSCC Immutep was granted Fast Track designation for efti to treat 1st line HNSCC patients by the US FDA in early April 2021. ... Jul 12
	LYNPARZA (olaparib) Approved in China for the Treatment of Certain Patients with BRCA-Mutated Metastatic Castration-Resistant Prostate Cancer Only PARP Inhibitor to Demonstrate Overall Survival Versus New Hormonal Treatments in BRCA1/2-Mutated Advanced Prostate Cancer... Jun 24
	Koselugo approved in the EU for children with neurofibromatosis type 1 and plexiform neurofibromas First medicine approved in the EU to treat this rare and debilitating genetic condition... Jun 22
	GSK and iTeos Therapeutics announce development and commercialisation collaboration for EOS-448 With this collaboration GSK is uniquely positioned with access to antibodies that synergistically target all three known CD226 checkpoints - TIGIT, CD96 and PVRIG.... Jun 14
	Bristol Myers Squibb announces LAG-3-Blocking antibody Relatlimab and Nivolumab fixed-dose Combination Significantly improves progression-free Survival vs. Opdivo (nivolumab) in patients... May 22
	GSK and Vir Biotechnology starts EMA rolling review of VIR-7831 (sotrovimab) for treatment of COVID-19 GSK's Covid product could be soon in the market after the emergency medical application review... May 11
	Roche’s Tecentriq approved by European Commission for metastatic non-small cell lung cancer Tecentriq is now the first and only single-agent cancer immunotherapy with three dosing options... May 08
	GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19 The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ... Mar 27
	GSK and Vir Biotechnology requests emergency use authorization to FDA for VIR-7831 for treatment of COVID-19 The FDA EUA submission is based on an interim analysis of efficacy and safety data from the Phase 3 COMET-ICE ... Mar 27
	Intra-Cellular Therapies Applies for FDA Approval of CAPLYTA (lumateperone) CAPLYTA (lumateperone)is indicated for the treatment of Bipolar Depression... Feb 23
	NMPA Approves Toripalimab in patients with recurrent or metastatic Nasopharyngeal Carcinoma Approval comes after Failure of at Least Two Lines of Prior Systemic Therapy... Feb 22
	Compugen expands clinical collaboration agreement with Bristol Myers Squibb Compugen Ltd expands collaboration agreement with Bristol Myers Squibb with phase 1b combination study of COM701 with opdivo C... Feb 22
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