Healthy Clinical Trial
Official title:
Relative Bioavailability of 40 mg/0.4 mL of BI 695501 Compared to 40 mg/0.8 mL of BI 695501 Formulation Following Single Subcutaneous Administration in Healthy Male and Female Subjects (a Double Blind, Randomised, Single-dose, Parallel-arm Study)
The main objective of this trial is to compare the pharmacokinetics (PK) of 40 mg BI 695501 100 mg/mL with 40 mg BI 695501 50 mg/mL following single subcutaneous administration.
n/a
NCT number | NCT05203289 |
Study type | Interventional |
Source | Boehringer Ingelheim |
Contact | Boehringer Ingelheim |
Phone | 1-800-243-0127 |
[email protected] | |
Status | Recruiting |
Phase | Phase 1 |
Start date | February 18, 2022 |
Completion date | August 30, 2022 |
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