A Phase I, Open Label, Multiple Dose, Dose Escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics and Antitumor Activities of Anti-BAFFR mAb(Monoclonal Antibody), ESG206 in Subjects With B-cell Lymphoid Malignancies
Latest Information Update: 25 Jul 2024
At a glance
- Drugs ESG 206 (Primary)
- Indications B-cell lymphoma
- Focus Adverse reactions
- Sponsors Shanghai Escugen Biotechnology
- 08 Aug 2023 Planned End Date changed from 1 Jan 2025 to 1 Mar 2025.
- 08 Aug 2023 Planned primary completion date changed from 1 Sep 2024 to 1 Nov 2024.
- 25 Jun 2023 Status changed from not yet recruiting to recruiting.