A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABBV-1088 Oral Dose in Healthy Adult Participants.
- Disease/Condition
- Healthy Volunteers
- Drug/Device/Intervention
- Drug: ABBV-1088
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- AbbVie
- Location
- Grayslake, United States of America
- Phase
- Phase 1
- Start date
- May 13, 2024
- End date
- Nov 28, 2024
- Enrollment
- 48 participants
Maximum Plasma Concentration (Cmax) of ABBV-1088,Time to Cmax (Tmax) of ABBV-1088,Terminal Phase Elimination Rate Constant (Beta) of ABBV-1088,Terminal Phase Elimination Half-Life (t1/2) of ABBV-1088,Area Under the Concentration-Time Curve From Time 0 to Time t (AUCt) of ABBV-1088,Area Under the Concentration-Time Curve From Time 0 to Infinity (AUCinf) of ABBV-1088,Number of Participants With Adverse Events (AEs)
This study will assess the single dose safety, tolerability and pharmacokinetic properties of
 ABBV-1088 in healthy adult participants
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06414798
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06414798 through Pure Global AI's free database. This Phase 1 trial is sponsored by AbbVie and is currently Not yet recruiting. The study focuses on Healthy Volunteers. Target enrollment is 48 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.