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A Phase 1 Study of ABBV-CLS-7262, Rosuvastatin, and Digoxin in Healthy Subjects

Phase 1
Waitlist Available
Research Sponsored by Calico Life Sciences LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up two weeks
Awards & highlights
No Placebo-Only Group

Summary

This trial tests how a new drug (ABBV-CLS-7262) interacts with common medications for cholesterol and heart conditions. Participants will take these drugs in different combinations to see how they work together.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~two weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and two weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Pharmacokinetics of Digoxin
Pharmacokinetics of Rosuvastatin
Secondary study objectives
Safety and Tolerability

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: ABBV-CLS-7262Experimental Treatment1 Intervention
ABBV-CLS-7262 + Digoxin + Rosuvastatin
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
ABBV-CLS-7262
2023
Completed Phase 1
~110

Find a Location

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

Calico Life Sciences LLCLead Sponsor
10 Previous Clinical Trials
927 Total Patients Enrolled
AbbVieIndustry Sponsor
1,035 Previous Clinical Trials
523,032 Total Patients Enrolled
~4 spots leftby Dec 2025