An Open-label, Dose Escalation and Expansion, Phase 1a/1b Study to Evaluate the Safety, Tolerability, Pharmacokinetics,Pharmacodynamics and Preliminary Antitumor Activity of TAK-500, a Novel Stimulator of Interferon Genes Agonist, as a Single Agent and in Combination With Pembrolizumab in Adult Patients With Select Locally Advanced or Metastatic Solid Tumors
Latest Information Update: 04 Sep 2024
At a glance
- Drugs Pembrolizumab (Primary) ; TAK-500 (Primary)
- Indications Adenocarcinoma; Advanced breast cancer; Gastric cancer; Head and neck cancer; Liver cancer; Mesothelioma; Nasopharyngeal cancer; Non-small cell lung cancer; Oesophageal cancer; Pancreatic cancer; Renal cell carcinoma; Solid tumours; Squamous cell cancer; Triple negative breast cancer
- Focus Adverse reactions
- Sponsors Takeda
- 20 Nov 2023 Change in phase,design term, treatment arms,timeframe of primary endpointsand addition of ORR endpoint.
- 20 Nov 2023 Planned number of patients changed from 118 to 313.
- 20 Nov 2023 Planned End Date changed from 20 Mar 2025 to 11 Aug 2026.