COMPLETED

A Study of Oral YUQ-A1007 in Healthy Volunteers

Conditions

Healthy Phase I Randomized Placebo-Controlled Sequential Escalation Safety Tolerability Pharmacokinetics YUQ-A1007 Healthy Volunteers

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

YUQ-A1007 is a novel gut-enriched AhR agonist. The nonclinical pharmacology study indicated that YUQ-A1007 has the potential to treat IBD. YUQ-A1007 has not been evaluated in human clinical studies. This study is first-in-human (FIH) study of YUQ-A1007. The goal of this trial is to evaluate the safety, tolerability, and pharmacokinetics of oral YUQ-A1007.

Official Title

A Phase I, Randomized, Placebo-Controlled, Sequential Single and Multiple Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Oral YUQ-A1007 in Healthy Volunteers

Quick Facts

Study Start:2025-03-20

Study Completion:2025-09-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT06835296

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 65 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Written informed consent prior to the conduct of any study-related assessments. 2. Aged 18 to 65 years, inclusive, at the time of signing the informed consent form (ICF). 3. Male and Female participants. 4. Has body mass index (BMI) as 18.5-27.9 kg/m2 with total body weight ≥ 50 kg for male participants and ≥ 45 kg for female participants at screening. 5. With normal liver and kidney functions. 6. With normal results of clinical laboratory tests or abnormal results of clinical laboratory tests deemed not clinically significant as per investigator judgement at screening and on admission to the CRU. 7. Willing and able to comply with the study requirements, including remaining at the CRU for the in-house portion of study participation. 8. Agrees not to smoke, vape, or consume tobacco or other nicotine-containing products, not to consume alcohol, not to consume beverages containing caffeine or other xanthines. 9. Is in good health based on the medical history, physical examination, vital signs measurements, laboratory tests, and 12-lead ECGs performed at screening.	1. Any condition that places the participant at significantly increased risk or may compromise the study objectives. 2. Is mentally or legally incapacitated at screening. 3. History of malignant neoplasms or carcinoma in situ. 4. Has a current or chronic history of liver disease or known hepatic or biliary abnormalities. 5. Has had symptomatic herpes zoster. 6. Has a history of any known relevant allergy/hypersensitivity or intolerance. 7. Has clinically significant multiple or severe drug allergies, intolerance to topical corticosteroids, or severe post-treatment hypersensitivity reactions. 8. Has a sensitivity to heparin or history of heparin-induced thrombocytopenia. 9. Has a clinically significant infection. 10. Any history of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological. 11. Has a clinically significant medical condition that, in the investigator's opinion, would preclude participation in the study. 12. Any clinically significant abnormality identified in the physical examination (including vital signs) or electrocardiographic testing. 13. Has a positive test for the presence of human immunodeficiency virus (HIV), hepatitis C antibody, hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) at screening or within 3 months prior to the first dose of investigational product. 14. Has active or latent tuberculosis (TB), regardless of treatment history, or positive diagnostic TB test at screening. 15. Has received treatment with a live, attenuated vaccine within 4 weeks prior to the first dose of investigational product or anticipation of need for such a vaccine during study participation. 16. Has a contraindication to blood sampling or is considered to have insufficient peripheral venous access. 17. Has donated or lost blood or blood products in volumes of 450 mL or more within 30 days. 18. Has had prior exposure to YUQ-A1007. 19. Has participated in a study of any investigational drug, device, biologic, or other agent within 30 days or 5 half-lives prior to screening, whichever is longer. 20. Has received any prescription medications, over-the-counter medications, herbal supplements, or vitamins within 30 days or 5 half-lives, whichever is longer, prior to the first dose of investigational product. 21. Is an employee or has a family member who is an employee of the CRU and is involved in the conduct of the study and/or supervised by the investigator; or is an employee or has a family member who is an employee of the sponsor.

Inclusion Criteria

Exclusion Criteria

1. Written informed consent prior to the conduct of any study-related assessments.
2. Aged 18 to 65 years, inclusive, at the time of signing the informed consent form (ICF).
3. Male and Female participants.
4. Has body mass index (BMI) as 18.5-27.9 kg/m2 with total body weight ≥ 50 kg for male participants and ≥ 45 kg for female participants at screening.
5. With normal liver and kidney functions.
6. With normal results of clinical laboratory tests or abnormal results of clinical laboratory tests deemed not clinically significant as per investigator judgement at screening and on admission to the CRU.
7. Willing and able to comply with the study requirements, including remaining at the CRU for the in-house portion of study participation.
8. Agrees not to smoke, vape, or consume tobacco or other nicotine-containing products, not to consume alcohol, not to consume beverages containing caffeine or other xanthines.
9. Is in good health based on the medical history, physical examination, vital signs measurements, laboratory tests, and 12-lead ECGs performed at screening.

1. Any condition that places the participant at significantly increased risk or may compromise the study objectives.
2. Is mentally or legally incapacitated at screening.
3. History of malignant neoplasms or carcinoma in situ.
4. Has a current or chronic history of liver disease or known hepatic or biliary abnormalities.
5. Has had symptomatic herpes zoster.
6. Has a history of any known relevant allergy/hypersensitivity or intolerance.
7. Has clinically significant multiple or severe drug allergies, intolerance to topical corticosteroids, or severe post-treatment hypersensitivity reactions.
8. Has a sensitivity to heparin or history of heparin-induced thrombocytopenia.
9. Has a clinically significant infection.
10. Any history of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological.
11. Has a clinically significant medical condition that, in the investigator's opinion, would preclude participation in the study.
12. Any clinically significant abnormality identified in the physical examination (including vital signs) or electrocardiographic testing.
13. Has a positive test for the presence of human immunodeficiency virus (HIV), hepatitis C antibody, hepatitis B surface antigen (HBsAg) or hepatitis B core antibody (HBcAb) at screening or within 3 months prior to the first dose of investigational product.
14. Has active or latent tuberculosis (TB), regardless of treatment history, or positive diagnostic TB test at screening.
15. Has received treatment with a live, attenuated vaccine within 4 weeks prior to the first dose of investigational product or anticipation of need for such a vaccine during study participation.
16. Has a contraindication to blood sampling or is considered to have insufficient peripheral venous access.
17. Has donated or lost blood or blood products in volumes of 450 mL or more within 30 days.
18. Has had prior exposure to YUQ-A1007.
19. Has participated in a study of any investigational drug, device, biologic, or other agent within 30 days or 5 half-lives prior to screening, whichever is longer.
20. Has received any prescription medications, over-the-counter medications, herbal supplements, or vitamins within 30 days or 5 half-lives, whichever is longer, prior to the first dose of investigational product.
21. Is an employee or has a family member who is an employee of the CRU and is involved in the conduct of the study and/or supervised by the investigator; or is an employee or has a family member who is an employee of the sponsor.

Contacts and Locations

Study Locations (Sites)

Anaheim Clinical Trials

Anaheim, California, 92801

United States

Collaborators and Investigators

Sponsor: Allianthera (Suzhou) Biopharmaceuticals Co., Ltd.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-03-20

Study Completion Date2025-09-30

Study Record Updates

Study Start Date2025-03-20

Study Completion Date2025-09-30

Terms related to this study

Keywords Provided by Researchers

Phase I
Randomized
Placebo-Controlled
Sequential Escalation
Safety
Tolerability
Pharmacokinetics
YUQ-A1007
Healthy Volunteers

Additional Relevant MeSH Terms

Healthy