MedPath

PRODUCTOS ROCHE S.A.Q. e I.

🇦🇷Argentina
Ownership
-
Employees
-
Market Cap
-
Website

Clinical Trials

151

Active:137
Completed:3

Trial Phases

3 Phases

Phase 1:28
Phase 2:2
Phase 3:6

Drug Approvals

40

SFDA:40

Drug Approvals

XELODA 500MG TABLET

Approval Date
Jul 18, 2025
Company
productose roche , s.a. de c.v
SFDA

TILCOTIL TAB 20MG

Approval Date
Jul 18, 2025
SFDA

HEMLIBRA 150 MG/ML SOLUTION FOR INJECTION

Approval Date
Jul 18, 2025
Company
chugai pharmaceutical co ltd
SFDA

ESBRIET 267 MG FILM COATED TABLET

Approval Date
Jul 18, 2025
Company
delpharm milano sri
SFDA

ESBRIET 801 MG FILM COATED TABLET

Approval Date
Jul 18, 2025
Company
delpharm milano sri
SFDA

RIVOTRIL 2.5MG-ML ORAL SOLUTION

Approval Date
Jul 18, 2025
Company
delpharm milano s.r.l
SFDA

XELODA 150MG TABLET

Approval Date
Jul 18, 2025
Company
productose roche , s.a. de c.v
SFDA

HERCEPTIN 150MG VIAL

Approval Date
Jul 18, 2025
SFDA

ACTEMRA 20 MG/ML Solution for injection/infusion

Approval Date
Jul 18, 2025
Company
chugai pharmaceutical co ltd
SFDA

ACTEMRA 20 MG/ML Solution for injection/infusion

Approval Date
Jul 18, 2025
Company
chugai pharmaceutical co ltd
SFDA
  • Prev
  • 1
  • 2
  • 3
  • 4
  • Next

Clinical Trials

Distribution across different clinical trial phases (36 trials with phase data)• Click on a phase to view related trials

Phase 1
28 (77.8%)
Phase 3
6 (16.7%)
Phase 2
2 (5.6%)
No trials found

News

GSK's TIM-3 Inhibitor Cobolimab Fails Phase III Trial in Advanced Lung Cancer

GSK's anti-TIM-3 monoclonal antibody cobolimab failed to improve overall survival in the Phase III COSTAR trial for advanced non-small cell lung cancer patients previously treated with immunotherapy.

IsoBio Secures $5 Million Series Seed Funding to Advance Antibody-Isotope Conjugates for Cancer Treatment

IsoBio, Inc. has closed a $5 million Series Seed financing round led by ASP Isotopes Inc. to develop antibody-isotope conjugates (AICs) targeting both validated and novel tumor antigens for cancer treatment.

European Regulators Recommend Expanding Novo Nordisk's Alhemo for Hemophilia A and B Without Inhibitors

The European Medicines Agency's Committee for Medicinal Products for Human Use issued a positive opinion recommending label expansion of Alhemo (concizumab) to treat severe hemophilia A and moderate/severe hemophilia B without inhibitors.

EU Regulatory Approval Advances Pfizer-BioNTech LP.8.1-Adapted COVID-19 Vaccine for 2025-2026 Season

The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended approval for Pfizer and BioNTech's LP.8.1-adapted COMIRNATY vaccine targeting XFG and NB.1.8.1 variants.

Roche Explores Direct-to-Consumer Drug Sales Model to Reduce US Patient Costs

Roche is considering selling prescription medicines directly to US consumers to lower patient costs, following government pressure to reduce drug prices.

Flatiron Health Triples Global Oncology Research Network, Expanding Real-World Data Access Across Three Countries

Flatiron Health's international oncology research network has tripled in size over the past year, now encompassing more than 30 partnerships across the UK, Germany, and Japan.

IXICO Secures Full Data Rights to Landmark Bio-Hermes-002 Alzheimer's Study Through Strategic GAP Partnership

IXICO has deepened its collaboration with the Global Alzheimer's Platform Foundation through an agreement securing full data usage rights to the Bio-Hermes-002 study, one of the most prominent global studies in Alzheimer's disease research.

Roche's Astegolimab Shows Mixed Results in COPD Trials, Phase IIb Study Meets Primary Endpoint

Roche's pivotal Phase IIb ALIENTO study met its primary endpoint, showing astegolimab reduced annualized exacerbation rate by 15.4% in COPD patients at 52 weeks.

BioNTech Chief Strategy Officer Ryan Richardson to Step Down After Seven-Year Tenure

Ryan Richardson will step down as Chief Strategy Officer from BioNTech's Management Board on September 30, 2025, after serving since January 2020.

Moleculin Appoints Roche Veteran Adriano Treve as Strategic Advisor Ahead of Phase 3 AML Trial Data

Moleculin Biotech has appointed Adriano Treve, a 40-year Roche veteran, as Strategic Advisor for partnerships as the company approaches key milestones in its Phase 3 MIRACLE trial.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.