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相关临床试验
4
3 进行中
药物批准
0
批准总数
监管机构
监管机构数
成立时间
N/A
进行中(未招募)
1
25.0%
已完成
尚未招募
2
50.0%
暂无批准数据
- Oral RT-114 delivered via RaniPill Capsule achieved systemic exposure greater than 150% relative to a matched 12 mg subcutaneous dose of PG-102 in a 30-person Phase 1a study. - Elimination half-life was nearly identical between oral (5.6 days) and subcutaneous (5.3 days) arms, suggesting intact peptide delivery into systemic circulation. - No adverse events were attributed to the RaniPill Capsule device; treatment-related events were mild, transient, and consistent with the GLP-1/GLP-2 agonist class. - The Phase 1a study is being expanded with a 15-person cohort to further characterize dose-concentration relationships before a Phase 1b obesity study expected to begin in 2026.