A PHASE 1, RANDOMIZED, DOUBLE-BLIND, THIRD-PARTY OPEN, PLACEBO-CONTROLLED STUDY TO EVALUATE THE PHARMACOKINETICS, SAFETY AND TOLERABILITY FOLLOWING SINGLE SUBCUTANEOUS DOSE OF PF-06480605 IN CHINESE HEALTHY PARTICIPANTS
Latest Information Update: 25 Mar 2024
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At a glance
- Drugs RVT-3101 (Primary)
- Indications Inflammatory bowel diseases; Ulcerative colitis
- Focus Adverse reactions; Pharmacokinetics
- Sponsors Pfizer
- 09 Jun 2022 Status changed from active, no longer recruiting to completed.
- 18 May 2022 Planned End Date changed from 8 Oct 2022 to 29 Oct 2022.
- 18 May 2022 Planned primary completion date changed from 8 Oct 2022 to 29 Oct 2022.