SHR-2106
/ Jiangsu Hengrui Pharma
- LARVOL DELTA
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August 27, 2026
A phase I clinical study of the safety, tolerability, pharmacokinetics and pharmacodynamics of SHR-2106, an anti-CD40 antibody, following single intravenous or subcutaneous administration in healthy participants.
(PubMed, Eur J Pharmacol)
- "SHR-2106 was well tolerated and achieved rapid and sustained CD40 engagement, supporting dose and route selection for Phase II studies."
Clinical • First-in-human • Journal • P1 data • PK/PD data • CD40LG
June 11, 2026
Safety and Tolerance of Increased Doses of SHR-2106 Injection in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=52 | Completed | Sponsor: Guangdong Hengrui Pharmaceutical Co., Ltd | Enrolling by invitation ➔ Completed
Trial completion • Transplantation
November 15, 2023
Safety and Tolerance of Increased Doses of SHR-2106 Injection in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=58 | Enrolling by invitation | Sponsor: Guangdong Hengrui Pharmaceutical Co., Ltd | Not yet recruiting ➔ Enrolling by invitation
Enrollment open • Transplantation
July 17, 2023
Safety and Tolerance of Increased Doses of SHR-2106 Injection in Healthy Subjects
(clinicaltrials.gov)
- P1 | N=58 | Not yet recruiting | Sponsor: Guangdong Hengrui Pharmaceutical Co., Ltd
New P1 trial • Transplantation
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