New drug interaction study aims to make atumelnant safer
NCT ID NCT07570082
First seen Jun 25, 2026 · Last updated Aug 20, 2026 · Updated 5 times
Summary
This study is testing how a new drug called atumelnant interacts with other medications in 46 healthy adults. Participants will receive atumelnant along with drugs like carbamazepine, midazolam, digoxin, and metformin to see how the body processes them. The goal is to gather safety and dosing information, not to treat any disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Atumelnant (also known as CRN04894), carbamazepine, midazolam, digoxin, metformin
- What this could lead to
- If successful, this study will help doctors understand how to safely dose atumelnant with other medications, reducing the risk of harmful drug interactions.
- What could go wrong
- This is an early-phase trial in healthy volunteers, not patients. The results may not predict effects in people with diseases, and drug interactions could still occur in real-world use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
46 people
The number who actually took part.
- Started
-
May 2026
- Finished
-
Jul 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
19 to 55 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Healthy adult females of non-childbearing potential (Section 14.2) or healthy adult males, 19-55 years of age, inclusive, at the screening visit. 2. BMI ≥18.0 and ≤32.0 kg/m2 at the screening visit. 3. Is willing and able to comply with all study procedures and restrictions, including fasting and consumption of protocol-specified standardized meal for required study measurements; inpatient admission; follow-up contact; receipt of rescue therapy, if necessary; abstinence from tobacco, alcohol, drugs, and from strenuous unaccustomed exercise and sports (defined as greater than 30 minutes per day) during the study period. 4. Normal adrenocorticotropic hormone (ACTH)-stimulated cortisol test at the screening visit and does not have signs and symptoms of adrenal insufficiency as deemed by the PI or designee. Exclusion Criteria: 1. Is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or expected during the conduct of the study. 2. History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI or designee. 3. Female participant with a positive pregnancy test at the screening visit or at first check-in or who is lactating. 4. Female participant of childbearing potential. 5. Had prior treatment with atumelnant. 6. Participation in another clinical study within 30 days or received any investigational drug within 5 half-lives prior to the first dosing, whichever is longer. The time window will be derived from the date of the last blood collection or dosing, whichever is later, in the previous study to Day 1 of the current study. 7. History or presence of hypersensitivity or idiosyncratic reaction to the study interventions or related compounds. 8. Has a blood loss ≥500 mL or donated blood within 3 months prior to the first dosing. 9. Unable to refrain from or anticipates the use of any drugs, including prescription and non-prescription medications, herbal remedies, vitamin supplements, or other food supplements within 14 days or 5 half-lives prior to the first dosing, whichever is longer.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Crinetics Study Site
Lincoln, Nebraska, 68502, United States
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