News about Global Pharma

Avixgen, US Biotech Firm Ink USD 360 Mn Deal for Next-Gen Drug Delivery Platform

Avixgen, US Biotech Firm Ink USD 360 Mn Deal for Next-Gen Drug Delivery Platform

Avixgen has signed a licensing-out agreement worth approximately USD 360 million with a US biotechnology company for its next-generation drug delivery platform, ACP (Advanced Cell Penetrating Peptide).

Global Pharma | 19/08/2025 | By Dineshwori 324

Skyhawk Therapeutics, Merck KGaA Darmstadt, Germany Partner to Develop RNA-Targeting Therapies for Neurological Disorders

Skyhawk Therapeutics, Merck KGaA Darmstadt, Germany Partner to Develop RNA-Targeting Therapies for Neurological Disorders

Skyhawk Therapeutics has entered a strategic research collaboration worth over USD 2 billion with Merck KGaA, Darmstadt, Germany to develop novel RNA-targeting small molecules for neurological disorders.

Global Pharma | 19/08/2025 | By Mrinmoy Dey 264

Glenmark Pharmaceuticals to Launch Micafungin for Injection in US in September 2025

Glenmark Pharmaceuticals to Launch Micafungin for Injection in US in September 2025

Glenmark Pharmaceuticals Inc., USA has announced the September 2025 launch of Micafungin for Injection USP, 50 mg and 100 mg vials, the bioequivalent of Astellas Pharma’s Mycamine.

Global Pharma | 19/08/2025 | By Mrinmoy Dey 282

Remegen Partners with Santen To Commercialise RC28-E in Greater China and Asian Countries

Remegen Partners with Santen To Commercialise RC28-E in Greater China and Asian Countries

RemeGen, a leading Chinese biopharmaceutical company, has entered into an exclusive licensing agreement for the ophthalmic innovative drug RC28-E with Santen China, a wholly-owned subsidiary of Santen Pharmaceutical.

Global Pharma | 19/08/2025 | By Dineshwori 413

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 228

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 515

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 210

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 257

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 383

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 625

 
 

 

 

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