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Merck Partners with Blackstone to Advance Development of Investigational Cancer Therapy Sacituzumab Tirumotecan

Merck Partners with Blackstone to Advance Development of Investigational Cancer Therapy Sacituzumab Tirumotecan

Under the agreement, Blackstone will provide Merck with USD 700 million in non-refundable funding to support a portion of the development costs expected through 2026.

| 05/11/2025 | By 261

Cipla to Acquire Inzpera Healthsciences for INR 110 Crore

Cipla to Acquire Inzpera Healthsciences for INR 110 Crore

Cipla Limited has announced that it will acquire a 100 percent stake in Inzpera Healthsciences Limited for a total consideration of approximately INR 110 crore.

| 05/11/2025 | By 502

Roche's Gazyva/Gazyvaro Shows Positive Results for Systemic Lupus Erythematosus in Phase III trials

Roche's Gazyva/Gazyvaro Shows Positive Results for Systemic Lupus Erythematosus in Phase III trials

The ALLEGORY study met its primary endpoint showing a higher percentage of people achieved a minimum four-point improvement in SLE Responder Index 4 (SRI-4) at one year (52 weeks) with Gazyva/Gazyvaro versus standard therapy.

| 05/11/2025 | By 359

Eli Lilly Investing USD 3 Billion in New Netherlands Facility to Boost Oral Medicine Manufacturing Capacity

Eli Lilly Investing USD 3 Billion in New Netherlands Facility to Boost Oral Medicine Manufacturing Capacity

Eli Lilly has announced plans to invest USD 3 billion in a new manufacturing facility in Katwijk, the Netherlands, to expand its global capacity for producing oral medicines and strengthen its supply chain network.

| 04/11/2025 | By 310

PBS Biotech Appoints Martin Simonetti as CEO

PBS Biotech Appoints Martin Simonetti as CEO

Simonetti is a veteran biotech executive who brings more than 40 years' industry expertise and leadership to PBS Biotech, including C-suite leadership, public and private financing and executing large-scale pharmaceutical collaborations.

| 04/11/2025 | By 347

Merz Aesthetics Unveils Ergonomically Designed Belotero Syringe for Enhanced Precision and Comfort

Merz Aesthetics Unveils Ergonomically Designed Belotero Syringe for Enhanced Precision and Comfort

The syringe has been engineered to provide greater precision, comfort, and control, enhancing the overall treatment experience for both practitioners and patients. It will first be introduced in Europe before a phased rollout across global markets.

| 04/11/2025 | By 236

Kimberly-Clark to Acquire Tylenol Maker Kenvue in Over 40 Billion Dollar Deal

Kimberly-Clark to Acquire Tylenol Maker Kenvue in Over 40 Billion Dollar Deal

Kimberly-Clark has announced plans to acquire Kenvue, the company behind Tylenol and other well-known consumer health brands, in a cash-and-stock transaction valued at approximately 48.7 billion dollars.

| 04/11/2025 | By 292

AIxMed and PathNet Partner to Advance Digital Pathology with AI-Driven Urine Cytology

AIxMed and PathNet Partner to Advance Digital Pathology with AI-Driven Urine Cytology

AIxMed has partnered with PathNet to advance digital pathology through its AIxURO solution, an AI-powered platform designed to enhance the analysis of non-invasive urine cytology samples. The collaboration aims to boost diagnostic accuracy and streamline workflows in bladder cancer detection.

| 04/11/2025 | By 294

Johnson & Johnson MedTech Confirms Durability of IVL in Complex Below-the-Knee Lesions in PAD Patients

Johnson & Johnson MedTech Confirms Durability of IVL in Complex Below-the-Knee Lesions in PAD Patients

Johnson & Johnson MedTech has released the one-year results of its DISRUPT BTK II study, reaffirming the safety and durability of the Shockwave Peripheral Intravascular Lithotripsy (IVL) System for the treatment of calcified below-the-knee (BTK) lesions in patients with peripheral artery disease (PA

| 04/11/2025 | By 277

UCB Wins FDA Approval for KYGEVVI, First-Ever Treatment for Thymidine Kinase 2 Deficiency

UCB Wins FDA Approval for KYGEVVI, First-Ever Treatment for Thymidine Kinase 2 Deficiency

UCB, the Brussels-based multinational biopharmaceutical company, has received approval from the US Food and Drug Administration (FDA) for KYGEVVI (doxecitine and doxribtimine), marking the first and only approved treatment for thymidine kinase 2 deficiency (TK2d) in adults and pediatric patients whose symptoms began at or before 12 years of age.

| 04/11/2025 | By 366

 
 

 

 

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