A Research Study Looking at a Single Dose of Etavopivat in Healthy Chinese Participants

NCT06581627 | Completed Phase 1

• 2 other identifiers: NN7535-7704U1111-1294-7463
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 1

Brief Summary

The study tests a new medicine called etavopivat in healthy Chinese participants. During the study, the participant will be given 1 dose of the study medicine. A dose is 2 tablets which are swallowed together with a cup of water. The study doctor will measure how much of the study medicine is in the blood as time passes. After the dose is given, the study will last for 7 to 9 days. The participants will attend a screening visit 2 to 28 days before they are given the study medicine. The participant will have 6 clinic visits in total. As part of the study, participant will stay overnight at the clinic for 3 nights. In some cases the doctor may decide that participant need to stay more nights. Participant will have blood tests and other health assessments at all 6 visits. Women cannot take part if pregnant, breast-feeding or plan to get pregnant during the study period. If the participant do take part in the study, participant will need to refrain from certain activities and behaviours for up to 3 months before taking the study medicine. Participant will also need to go without food and drinks other than water in the 10 hours before and 4 hours after taking the medicine.

Conditions

Healthy Volunteers; Sickle Cell Disease; Thalassemia

Outcome Measures

Primary Outcomes (9)

• AUC0-inf,etavopivat: Area under the etavopivat plasma concentration-time curve from 0 hours and extrapolated to infinity after a single dose

  Measured in hour\*nanogram/millilitre (h\*ng/mL).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• Cmax,etavopivat: Maximum observed etavopivat plasma concentration after a single dose

  Measured in nanograms/millilitre (ng/mL).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• Weight-adjusted AUC0-inf,etavopivat: Area under the etavopivat plasma concentration-time curve from 0 hours and extrapolated to infinity after a single dose divided by body weight

  Measured in(hour\*nanogram/millilitre)/kilograms ((h\*ng/mL)/kg).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• Weight-adjusted Cmax,etavopivat: Maximum observed etavopivat plasma concentration after a single dose divided by body weight

  Measured in (nanograms/millilitre )/kilogram ((ng/mL)/kg).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• AUC0-last,etavopivat: Area under the etavopivat plasma concentration-time curve from0 hours to the time of last quantifiable concentration

  Measured in hour\*nanogram/millilitre (h\*ng/mL).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• tmax,etavopivat: Time to maximum observed etavopivat plasma concentration after a single dose

  Measured in hour (h).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• t½,etavopivat: Terminal half-life for etavopivat after a single dose

  Measured in hour (h).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• CL/F etavopivat: Apparent plasma clearance of etavopivat after a single dose

  Measured in Litre/hour (L/h).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

• Vz/F etavopivat: Apparent volume of distribution of etavopivat after a single dose based on plasma concentration values

  Measure in litre (L).

  From 0 to 120 hours after investigational medicinal product (IMP) administration (day 6)

Secondary Outcomes (1)

• Number of adverse events

  From dosing (day 1) to end of study (day 7 to 9)

Study Arms (1)

Etavopivat

EXPERIMENTAL

Participants will be administered a single dose of 2 tablets of etavopivat together.

Drug: Etavopivat

Interventions

Etavopivat DRUG

2 tablets of Etavopivat will be administered in fasted state via oral route

Etavopivat

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Male or female Chinese participants.
• Age 18-45 years (both inclusive) at the time of signing the informed consent form.
• Body mass index (BMI) between 18.0 and 33.0 kg/m\^2 (both inclusive) at screening.
• Body weight greater than or equal to 40.0 kg at screening.
• Considered to be generally healthy based on the medical history, physical examination and the results of vital signs, electrocardiogram (ECG) and clinical laboratory tests performed during the screening visit, as judged by the investigator.

You may not qualify if:

• Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using adequate contraceptive methods.
• Participation (i.e., signed informed consent) in any other interventional clinical study within 90 days or 5 times the half-life of the previous investigational medical product (IMP) (if known), whichever is longer before screening.
• Any disorder, unwillingness or inability, which in the investigator's opinion might jeopardise the participant's safety or compliance with the protocol.
• Use of any medication with unknown or unspecified content within 90 days before screening.
• Use of prescription medicinal products or non-prescription drugs (including Chinese traditional medicine or local medicine) within 14 days before screening, as declared by the participant, apart from:
• Acceptable contraceptive methods
• Hormone replacement therapy (for menopausal females)
• Over-the-counter topical medications known to not reach systemic circulation
• Occasional use of:
• Acetaminophen up to 2 grams (g) (4 x 0.5 g) daily
• Ibuprofen up to 2.4 g (4 x 0.6 g) daily
• Acetylsalicylic acid up to 2.4 g (4 x 0.6 g) daily
• Is unable to refrain from or anticipates the use of any drug known to be a strong or moderate inhibitor or inducer of uridine 5'-diphospho glucuronosyltransferase (UGT) enzymes, cytochrome P450 (CYP) 3A4, CYP2C9 or permeability glycoproteins (P-gp), including St. John's Wort, for 28 days prior to dosing and throughout the study
• Is unable to refrain from or anticipates the use of any medications or substances prohibited in the study
• Use of tobacco and nicotine products, defined as any of the following:

Sponsors & Collaborators

• Novo Nordisk A/S: lead

Study Sites (1)

Beijing Hospital

Beijing, Beijing Municipality, 100730, China

Location

MeSH Terms

Conditions

Anemia, Sickle Cell; Thalassemia

Condition Hierarchy (Ancestors)

Anemia, Hemolytic, Congenital; Anemia, Hemolytic; Anemia; Hematologic Diseases; Hemic and Lymphatic Diseases; Hemoglobinopathies; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Study Officials

• Clinical Transparency '(dept. 2834)'

  Novo Nordisk A/S

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 30, 2024
• First Posted: September 3, 2024
• Study Start: August 26, 2024
• Primary Completion: October 31, 2024
• Study Completion: October 31, 2024
• Last Updated: December 29, 2025

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will share

Locations

CN (1)