A Phase I Clinical Trial to Evaluate the Single Dose Ascending and Food Effects of PG-033 in Healthy Adults

NCT07013097 | Recruiting Phase 1

• 2 other identifiers: PG-033-ND-101CTR20251749
• Study Type: interventional
• Target: 52
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this study is to evaluate the safety, tolerability and pharmacokinetics (PK) profiles of single ascending oral doses(SAD) of PG-033 by directly comparing it with placebo. Meanwhile, the impact of a high-fat meal on the pharmacokinetics of PG-033 will also be evaluated. The research will also explore the potential metabolites and metabolic pathways of PG-033 within the human body，as well as investigate the effect of PG-033 on the QTc interval.

Conditions

Lichen Simplex Chronicus

Keywords

PG-033; Lichen Simplex Chronicus; Pruritus

Outcome Measures

Primary Outcomes (1)

• Safety and tolerability of PG-033 tablets

  Incidence of treatment-emergent adverse events (AEs) and serious adverse events (SAEs)

  Single Ascending Dose study: 7 days；Food Effect study: 14 days

Secondary Outcomes (10)

• Pharmacokinetics parameter: Cmax

  up to 3 days

• Pharmacokinetics Parameter:Tmax

  up to 3 days

• Pharmacokinetics parameter: AUC0-t

  up to 3 days

• Pharmacokinetics parameter: AUC0-∞

  up to 3 days

• Pharmacokinetics parameter: t1/2

  up to 3 days

Study Arms (2)

Single Ascending Doses of PG-033 tablets

ACTIVE COMPARATOR

Drug: PG-033

Placebo

PLACEBO COMPARATOR

Drug: PG-033 placebo comparator

Interventions

PG-033 DRUG

Oral tablets (2mg， 10mg)

Single Ascending Doses of PG-033 tablets

PG-033 placebo comparator DRUG

Oral tablets (2 mg, 10 mg) (matching corresponding study medication)

Placebo

Eligibility Criteria

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

You may qualify if:

• \. Read, understood, and signed an ICF before any investigational procedure(s) are performed.
• Male or female aged 18 to 45 (including threshold). 3. For male subjects, the body weight should be ≥ 50.0 kg, and for female subjects, the body weight should be ≥ 45.0 kg. The body mass index (BMI) should be within the range of 19.0 to 26.0 kg/m²(including threshold).
• \. Results of vital signs examination, physical examination, clinical laboratory tests (including blood routine examination, urine routine examination, blood biochemistry examination, coagulation function examination, thyroid function examination, etc.), chest X-ray, adrenal gland color ultrasound, etc. during the screening period show normal results or, if there are abnormalities, they are judged by the investigator to have no clinical significance.
• \. Be willing to avoid pregnancy or voluntarily take effective contraceptive measures and have no sperm or egg donation plan from the signing of the informed consent form to three month after the last administration of the investigational medicinal product.
• \. Be able to communicate well with the investigator and understand and comply with the requirements of the study.

You may not qualify if:

• \. Participants with abnormal electrocardiogram results during screening (e.g., QT/QTcF \> 440 ms, PR interval \> 200 ms, QRS complex duration \> 100 ms, clinically significant abnormalities of the P wave, clinically significant changes in the ST-T wave, etc.).
• \. Participants known to be allergic to this product or related excipients; or participants with an allergic constitution (such as those who are allergic to two or more drugs or foods).
• \. Participants with a history of chronic diseases or severe diseases in the circulatory, urinary, respiratory, hematological and lymphatic, endocrine, immune, mental and neurological, digestive systems, etc.
• \. Participants who have undergone major surgery within 6 months before the first dose administration, or those who plan to have surgery during the study period, or those who have undergone surgery that, as judged by the investigator, will affect the evaluation of the drug's safety and pharmacokinetic characteristics.
• \. Participants who have used any drugs (including any prescription drugs, over-the-counter drugs, traditional Chinese herbal medicines) and health products within 2 weeks before the first dose administration.
• \. Participants who have used any drugs that inhibit or induce the liver's metabolism of drugs (e.g., barbiturates, carbamazepine, phenytoin, glucocorticoids, omeprazole, selective serotonin reuptake inhibitors (SSRI) antidepressants, cimetidine, diltiazem, macrolides, nitroimidazoles, sedative-hypnotics, verapamil, fluoroquinolones, antihistamines, etc.) within 4 weeks before the first dose administration.
• \. Participants who are unable to stop consuming beverages and foods containing caffeine, alcohol, etc. (including chocolate, tea, coffee, cola, etc.), or foods that affect drug metabolism such as grapefruit, grapefruit products, pitaya, mango, pomelo, etc. from 48 hours before the first dose administration until the end of the trial, or those who are unable to stop consuming the above-mentioned diets from 48 hours before the first dose administration until the end of the trial.
• \. Participants who have received live attenuated vaccine vaccination within 4 weeks before the first dose administration or those who need to receive live attenuated vaccine vaccination during the trial.
• \. Participants with positive serological results for hepatitis B surface antigen (HBsAg), hepatitis C antibody, Treponema pallidum antibody, or human immunodeficiency virus antibody during screening.
• \. Participants who have participated in other clinical trials within 3 months before the first dose administration.
• \. Participants who have donated blood or lost a total of ≥ 400 mL of blood (excluding physiological blood loss in females) within 3 months before the first dose administration, received blood transfusion or used blood products, or those who plan to donate blood during the trial or within 1 month (30 days) after the end of the trial.
• \. Participants who have consumed an average of more than 2 units of alcohol per day within 30 days before screening (1 unit ≈ 360 mL of beer or 45 mL of liquor with an alcohol content of 40% or 150 mL of wine), or those who cannot abstain from alcohol during the trial, or those with a positive result in the alcohol breath test.
• \. Participants who have smoked an average of more than 5 cigarettes per day within 3 months before screening, or those who cannot stop smoking during the trial.
• \. Participants with a history of drug abuse within 1 year before screening or those who tested positive for drug abuse screening.
• \. Participants who cannot tolerate intravenous puncture/indwelling needle or those with a history of fainting at the sight of needles or blood.

Sponsors & Collaborators

• Prime Gene Therapeutics Co., Ltd.: lead

Study Sites (1)

Beijing Shijitan Hospital , Capital Medical University

Beijing, Beijing Municipality, 100038, China

RECRUITING

MeSH Terms

Conditions

Neurodermatitis; Pruritus

Condition Hierarchy (Ancestors)

Dermatitis; Skin Diseases; Skin and Connective Tissue Diseases; Skin Diseases, Eczematous; Skin Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Central Study Contacts

Xiaohua Hao Beijing Shijitan Hospital Affiliated to Capital Medical Univer

CONTACT

+86 13466590802; xiaohualuck@sina.com

Study Design

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

Study Record Dates

• First Submitted: May 19, 2025
• First Posted: June 10, 2025
• Study Start: May 23, 2025
• Primary Completion: October 31, 2025
• Study Completion: December 31, 2025
• Last Updated: June 10, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)