News about Global Pharma

Pilatus Biosciences Collaborates with Roche to Evaluate PLT012 in First-in-Human Study in Hepatocellular Carcinoma

Pilatus Biosciences Collaborates with Roche to Evaluate PLT012 in First-in-Human Study in Hepatocellular Carcinoma

Atezolizumab will be provided by Genentech for use in Pilatus’ clinical research; PLT012 is Pilatus’ immunomodulatory candidate.

Global Pharma | 18/08/2025 | By Abha 259

Marksans Pharma's UK Subsidiary Relonchem Secures Multiple MHRA Approvals

Marksans Pharma's UK Subsidiary Relonchem Secures Multiple MHRA Approvals

Marksans Pharma's wholly owned UK subsidiary, Relonchem Ltd., has received marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA) for Metformin Hydrochloride Relonchem Prolonged Release Tablets in three strengths—500 mg, 750 mg, and 1000 mg.

Global Pharma | 18/08/2025 | By Dineshwori 565

Kwality Pharma Receives Registration for Anti-Cancer Drug Bleomycin 15 IU In Mexico

Kwality Pharma Receives Registration for Anti-Cancer Drug Bleomycin 15 IU In Mexico

Kwality Pharmaceuticals has received product registration for Bleomycin 15 IU in Mexico for sale and distribution, expanding its oncology portfolio in regulated markets

Global Pharma | 18/08/2025 | By Dineshwori 223

UK Approves Sanofi's Teplizumab to Delay Onset of Stage 3 Type 1 Diabetes

UK Approves Sanofi's Teplizumab to Delay Onset of Stage 3 Type 1 Diabetes

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved teplizumab (Tzield) to delay the onset of Stage 3 type 1 diabetes (T1D) in adults and children aged 8 years and older with Stage 2 T1D.

Global Pharma | 18/08/2025 | By Dineshwori 275

Tonix Pharmaceuticals Secures FDA Nod for Tonmya, a First-in-Class Therapy for Fibromyalgia

Tonix Pharmaceuticals Secures FDA Nod for Tonmya, a First-in-Class Therapy for Fibromyalgia

Tonix Pharmaceuticals has received approval from the US Food and Drug Administration (FDA) for Tonmya (cyclobenzaprine HCl sublingual tablets) for the treatment of fibromyalgia in adults.

Global Pharma | 18/08/2025 | By Dineshwori 396

Alembic Secures Final USFDA Nod for Tretinoin Cream USP, 0.025%

Alembic Secures Final USFDA Nod for Tretinoin Cream USP, 0.025%

Alembic Pharmaceuticals has received final approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) for Tretinoin Cream USP, 0.025 percent, indicated for the treatment of acne vulgaris.

Global Pharma | 16/08/2025 | By Dineshwori 694

Novo Nordisk's Wegovy Approved for Treatment of MASH in Adults with Liver Fibrosis

Novo Nordisk's Wegovy Approved for Treatment of MASH in Adults with Liver Fibrosis

The US FDA has approved an additional indication for Wegovy (semaglutide 2.4 mg) for the treatment of noncirrhotic metabolic dysfunction-associated steatohepatitis (MASH) in adults with moderate to advanced liver fibrosis, according to Novo Nordisk.

Global Pharma | 16/08/2025 | By Dineshwori 386

Precigen Wins FDA Approval for PAPZIMEOS as First Immunotherapy for Recurrent Respiratory Papillomatosis

Precigen Wins FDA Approval for PAPZIMEOS as First Immunotherapy for Recurrent Respiratory Papillomatosis

US-based biopharmaceutical company Precigen has received approval from the Food and Drug Administration (FDA) for its immunotherapy PAPZIMEOS (zopapogene imadenovec-drba) for the treatment of adults with recurrent respiratory papillomatosis (RRP).

Global Pharma | 16/08/2025 | By Dineshwori 238

Vcare, Huadong Medicine Join Forces to Commercialise JAK1 Inhibitor VC005 Tablets in China

Vcare, Huadong Medicine Join Forces to Commercialise JAK1 Inhibitor VC005 Tablets in China

Jiangsu Vcare Pharmatech has entered an exclusive strategic partnership with Huadong Medicine to commercialize its innovative JAK1 inhibitor VC005 tablets for autoimmune diseases in China.

Global Pharma | 16/08/2025 | By Mrinmoy Dey 556

Shilpa Medicare Secures CDSCO Approval for NorUDCA Tablets in NAFLD Treatment

Shilpa Medicare Secures CDSCO Approval for NorUDCA Tablets in NAFLD Treatment

Shilpa Medicare Ltd has received approval from India's Central Drugs Standard Control Organization (CDSCO) for Nor Ursodeoxycholic Acid (NorUDCA) Tablets 500 mg for the treatment of Non-Alcoholic Fatty Liver Disease (NAFLD).

Global Pharma | 16/08/2025 | By Dineshwori 735

 
 

 

 

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