Fact CheckerSign in

NCT06527781CompletedPhase 1

A Study of PD5K3 in Healthy Adult Volunteers

A Phase 1a Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity of PD5K3 in Healthy Adult Volunteers

Source: ClinicalTrials.gov · Last updated 30 Jul 2024

Brief summary (registry, in English)

The main aim of this clinical trial is to assess the safety of PD5K3 in patients aged 18 to 65 years. The main questions it aims to answer are: * Is PD5K3 safe in adult? Researchers will compare PD5K3 to an active comparator pegaspargase to see if PD5K3 is safe and active in human. Participants will * Receive a single dose injection of PD5K3, pegaspargase or placebo according to weight, * Visit the clinic for assessment.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
28 (actual)
First submitted
19 Jul 2024
Start date
27 Nov 2023
Primary completion date
20 May 2024
Lead sponsor
Chongqing Peg-Bio Biopharm Co., Ltd.
NCT number
NCT06527781

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 28
  • From 27 Nov 2023 to the primary completion date, 20 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Used PEGylated drugs in the past;
  • Positive urine test for drug abuse;
  • Smoke excessively (average \> 5 cigarettes/day) within 3 months before screening or cannot stop using any tobacco products during the trial;
  • Drink excessively every day within 3 months before screening (male daily alcohol consumption exceeds 25g, such as 750 mL of beer, 250 mL of wine, or 75 mL of 38° liquor; female daily alcohol consumption exceeds 15g, such as 450 mL of beer, 150 mL of wine, or 50 mL of 38° liquor), or cannot abstain from alcohol during the trial;
  • Drink excessive amounts of tea, coffee or caffeinated beverages every day within 3 months before screening (more than 8 cups per day, 1 cup = 250 mL);
  • Undergone surgery within 3 months before screening or plan to undergo surgery during the trial;
  • Donated blood or lost more than 400 mL of blood within 3 months before screening (excluding menstrual bleeding);
  • Participated in any clinical trial as a subject within 3 months before screening;
  • Took any prescription drugs, over-the-counter drugs, health products, and any functional vitamins or Chinese herbal products within 28 days before administration;
  • The subject or his/her partner is unwilling to use one or more non-drug contraceptive measures (such as complete abstinence, condoms, contraceptive rings, ligation, etc.) for contraception during this trail or have a fertility plan within 6 months after the end of the study;

Other illness

  • Suffering from any diseases of the circulatory system, digestive system, urinary system, respiratory system, nervous system, endocrine system, reproductive system, etc. or any other diseases that can interfere with the test results;
  • Allergic constitution, including allergic to asparaginase;
  • Have difficulty in venous blood collection, have a history of needle phobia or blood phobia, or have a known severe bleeding tendency;
  • One or more positive tests for hepatitis B virus surface antigen, hepatitis C virus antibody, syphilis specific antibody, and human immunodeficiency virus antibody;

Lab values

  • Abnormal results with clinically significance of comprehensive physical examination, vital signs, laboratory tests (blood routine, blood biochemistry, seven coagulation items, urine routine, myocardial enzymes), 12-lead electrocardiogram, chest X-ray (anteroposterior), abdominal B-ultrasound (liver, gallbladder, pancreas, spleen and kidney);
  • Fasting blood glucose ≥ 6.1mmol/L;

Other

  • Positive breath test for alcohol;
  • Female subjects are in lactation or have positive blood pregnancy test during the screening period or trial;
  • The investigator believes the subject would be unsuitable for participation in this clinical study.

Who the study is looking for

  • Chinese healthy male or female subjects;
  • Aged 18 to 65 years (inclusive);
  • The body mass index (BMI) in the range 18.0\~28.0 kg/m\^2 (inclusive);
  • Voluntarily participate and sign the informed consent form;
  • Be able to complete the trial in accordance with the protocol.

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital of Soochow University
Coordinator of this site? Confirm its status
SuzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.