A Study to Assess Pharmacokinetics, Safety, and Tolerability of Atumelnant in Healthy Japanese and Caucasian Participants

NCT07221084 | Completed Phase 1 DMC FDA Drug

• 1 other identifier: CRN04894-153
• Study Type: interventional
• Target: 21
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to assess the PK profile, safety, and tolerability of atumelnant after single and multiple once daily (QD) oral doses in healthy Japanese and Caucasian adult participants.

Conditions

Healthy Volunteers

Keywords

Healthy Volunteers; CRN04894; Atumelnant

Outcome Measures

Primary Outcomes (3)

• Pharmacokinetics (Cmax)

  Assessment of the maximum observed plasma concentration of atumelnant

  [Time Frame: Up to Day 30]

• Pharmacokinetics (Tmax)

  Assessment of time to maximal atumelnant concentration (Tmax)

  [Time Frame: Up to Day 30]

• Pharmacokinetics (AUC)

  Assessment of the plasma area under the curve of Atumelnant

  [Time Frame: Up to Day 30]

Secondary Outcomes (6)

• Number of participants with Treatment Emergent Adverse Events including Adverse Events of Special Interest (adrenal insufficiency)

  [Time Frame: Up to Day 50]

• Number of participants with clinically significant clinical laboratory abnormalities

  [Time Frame: Up to Day 30]

• Number of participants with clinically significant changes in vital signs

  [Time Frame: Up to Day 30]

• Number of participants with clinically significant changes in physical exam observations

  [Time Frame: Up to Day 30]

• Number of participants with clinically significant Electrocardiogram (ECG) abnormalities

  [Time Frame: Up to Day 20]

Study Arms (4)

Treatment (Cohort 1)

EXPERIMENTAL

Fixed-sequence cohort for Japanese participants.

Drug: Atumelnant

Placebo (Cohort 1)

ACTIVE COMPARATOR

Fixed-sequence cohort for Japanese participants.

Drug: Placebo

Treatment (Cohort 2)

EXPERIMENTAL

Fixed-sequence cohort for Caucasian participants.

Drug: Atumelnant

Placebo (Cohort 2)

ACTIVE COMPARATOR

Fixed-sequence cohort for Caucasian participants.

Drug: Placebo

Interventions

Atumelnant DRUG

Atumelnant, tablets, once daily by mouth

Also known as: CRN04894

Treatment (Cohort 1); Treatment (Cohort 2)

Placebo DRUG

Placebo, tablets, once daily by mouth

Placebo (Cohort 1); Placebo (Cohort 2)

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy male or female participants, 18 to 55 years old, inclusive, at the Screening Visit.
• Healthy status as defined by the absence of evidence of any clinically significant, in the opinion of the Investigator, active or chronic disease following a detailed medical and surgical history, a complete physical examination including vital signs, 12-lead electrocardiogram (ECG), hematology, clinical chemistry, coagulation, serology, and urinalysis. The tests may be repeated once at Screening and at admission on Day -1 if necessary and deemed appropriate by the Investigator or designee.
• Body mass index (BMI) between 18.0 and 30.0 kg/m2, inclusive, at the Screening Visit and at admission on Day -1.
• Meeting the criteria at the time of consent for one of the following ethnic groups:
• Japanese participants must have been born in Japan to parents and grandparents of Japanese ethnic descent as evidenced by verbal confirmation and documented in a self-reported family tree form, have lived less than 10 years outside of Japan, and have no significant change in lifestyle, including diet, since leaving Japan.
• Caucasian participants must be considered White of European descent.
• Participant has a peak 30- or 60-minute ACTH stimulated serum cortisol ≥18 μg/dL during 250 μg high-dose ACTH/cosyntropin stimulation test conducted at Screening.
• Participant has normal morning serum cortisol collected at approximately 08:00 AM (±2 hours) at admission on Day -1 and does not have signs and symptoms of adrenal insufficiency as deemed by the Investigator or designee.

You may not qualify if:

• Participant is breastfeeding or has a positive serum pregnancy test at Screening or at admission on Day -1.
• Participant has a blood loss ≥500 mL or donated blood within 3 months prior to admission on Day -1.
• Participant has received atumelnant previously or has previously been enrolled in this clinical study.
• Participant has received any investigational drug within the past 30 days or 5 half lives, whichever is longer, prior to the first dose of study intervention on Day 1.
• Participant is unwilling to refrain from strenuous, unaccustomed exercise and sports, defined as greater than 30 minutes per day, 3 days prior to admission on Day -1.
• Participant has history of hypersensitivity to study intervention or any of the excipients or to medicinal products with similar chemical structures.
• Participant has used any prescription medication without approval of the Investigator or designee within 14 days prior to admission on Day -1. By exception, hormonal contraceptives are permitted throughout the study and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines are allowed up to 14 days prior to admission on Day -1.
• Venous access considered inadequate for sample collection.

Sponsors & Collaborators

• Crinetics Pharmaceuticals Inc.: lead

Study Sites (1)

Crinetics Study Site

Glendale, California, 91206, United States

Location

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 22, 2025
• First Posted: October 27, 2025
• Study Start: October 28, 2025
• Primary Completion: February 7, 2026
• Study Completion: February 27, 2026
• Last Updated: March 11, 2026

Record last verified: 2025-10

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)