An Open-label, First-in-human, Dose Escalation and Expansion Phase I Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Profile of JS201 in Patients With Advanced Malignant Tumors
Latest Information Update: 04 Aug 2023
At a glance
- Drugs JS 201 (Primary)
- Indications Solid tumours
- Focus Adverse reactions; First in man
- Sponsors Shanghai Junshi Biosciences
- 01 Apr 2022 Planned number of patients changed from 174 to 244.
- 30 Aug 2021 According to a Junshi Biosciences - Impact Therapeutics media release, in July 2021, first patient was dosed in this study.
- 03 Aug 2021 Planned End Date changed from 30 Dec 2022 to 7 Jul 2023.