ClinicalTrials.Veeva

Menu

A Phase 1b Study to Evaluate the Safety of XEN-101

X

Xeno Biosciences

Status and phase

Terminated
Phase 1

Conditions

Obesity

Treatments

Drug: XEN-101
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT06417697
XB-101-102

Details and patient eligibility

About

This Phase 1b study will evaluate the effects of XEN-101 in subjects with obesity

Full description

This study will assess the safety, tolerability and weight loss associated with XEN-101 in obese men and women.

Enrollment

33 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male or female, age 18 to 60 years, inclusive, at Screening
  2. Body mass index of 30 to 45 kg/m2
  3. Stable body weight for at least 3 months (i.e., fluctuation of ≤5%)
  4. If a female of childbearing potential, must agree to use double barrier contraception (e.g., condom and 1 additional form of adequate contraception) from the date of signing of the ICF, throughout the study, and for 4 weeks after the final dose of study drug. In addition, she must be advised not to donate ova during this period. If a non-sterilized male is sexually active with a female partner of childbearing potential, he must use double barrier contraception from the date of signing of the ICF, throughout the study, and for 8 weeks after the final dose of study drug. In addition, he must be advised not to donate sperm during this period
  5. If a female of childbearing potential, must have a negative pregnancy test at Screening and on Day 1 (baseline)
  6. Able to provide informed consent
  7. Willing and able to comply with this protocol and procedures, including feces collection, and be available for the entire duration of the study

Exclusion criteria

  1. Currently enrolled in another investigational device or drug study, or less than 30 days or 5 times the half-life of the drug candidate (whichever is longer) has passed between Screening for this study and the end of the Treatment Period of the previous investigational device or drug study
  2. Diagnosed with type 1 diabetes or type 2 diabetes (T2D) (resolution of T2D >3 years before Screening is allowed)
  3. Laboratory evidence during Screening of T2D, including glycated hemoglobin (HbA1c) ≥6.5% or fasting glucose ≥126 mg/dL (≥7.0 mmol/L)
  4. Evidence of clinically significant cardiac, neurologic, psychiatric, pulmonary, renal, hepatic, endocrine, metabolic, or gastrointestinal disease that, in the Investigator's opinion, would compromise the safety of the subject, interfere with the interpretation of the study results, or otherwise preclude subject participation
  5. Female who is pregnant, nursing, or intends to become pregnant during the study.
  6. Positive result for hepatitis B virus surface antigen, hepatitis C virus ribonucleic acid, and human immunodeficiency virus (HIV) antibody at Screening
  7. Use of anti-obesity medications (e.g., glucagon-like peptide-1 analogues, stimulants, bupropion/naltrexone) within 6 months before Screening

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

33 participants in 2 patient groups, including a placebo group

XEN-101
Experimental group
Treatment:
Drug: XEN-101
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

Loading...

Central trial contact

Dennis Kim, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems