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Phase 1 Completed N=32 Randomized Triple-blind Treatment

A Study of Single Ascending Doses of IW-3300 in Healthy Volunteers

Healthy Volunteers
Source: ClinicalTrials.gov NCT05188261 ↗
Enrolled (actual)
32
Serious AEs
0.0%
Results posted
Dec 2023
Primary outcomePrimary: Number of Participants With Treatment-Emergent Adverse Events (TEAEs) — 2; 1; 0; 1 Participants

Summary

This is a first-in-human study to evaluate the safety and tolerability of single ascending doses of IW-3300. The study drug will be administered rectally as a low-volume (20 mL) enema. Study participants will be randomized in a 3:1 ratio to receive a single dose of IW-3300 or placebo. Up to 5 different doses of IW-3300 will be studied. Safety reviews will be conducted before proceeding to each higher dose.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Treatment-Emergent Adverse Events (TEAEs)
2; 1; 0; 1; 2
PRIMARY
Number of Participants With Serious TEAEs
0; 0; 0; 0; 0

Eligibility Criteria

Inclusion Criteria

  • Males and female subjects of non-childbearing potential
  • Ages 18 to 60 years
  • Medically healthy with no clinically significant findings during medical evaluation including physical examination, 12-lead electrocardiogram (ECG), and clinical laboratory tests.
  • Normal bowel movement frequency of formed stool at baseline (≥3 per week and ≤3 per day; average Bristol stool form scale (BSFS) score of >2 and <6).
  • Body mass index (BMI) within the range 18.5 to 35.0 kg/m2 (inclusive) at the Screening Visit.
  • Male subjects and female partners are willing to use double-barrier method of contraception during the study.
  • If subject is ≥45 years of age, subject is compliant with colorectal cancer screening guidelines according to the American College of Gastroenterology (ACG) Clinical Guidelines: Colorectal Cancer Screening 2021.

Exclusion Criteria

  • Evidence or history of clinically significant acute or chronic disease, or clinically significant illness within 30 days of the Screening Visit.
  • History of clinically significant hypersensitivity or allergies to any of the inactive ingredients contained in the active or placebo drug products.
  • History of any condition that would interfere with their ability to receive an enema, or has had difficulty receiving an enema in the past.
  • Recent history of anal fissure, anal abscess, complicated hemorrhoids, or presence or history of inflammatory bowel disease.
  • Used a prescription medication during the 14 days before Check-in
  • Used any over-the-counter medications, including laxatives, and herbal supplements during the 7 days before Check-in.
  • Received a licensed or investigational vaccine during the 30 days before Check-in or is planning to receive any vaccine during the study.
  • Recently received or donated blood products.
  • Undergone a surgical procedure during the 30 days before Check-in, other than minor dermatologic procedures, or has a history of surgery involving the GI tract or anal canal (with the exception of endoscopic procedures, appendectomy, and cholecystectomy).
  • Received any investigational drug during the 30 days or 5 half-lives of that investigational drug (whichever is longer) before the Screening Visit, or is planning to receive another investigational drug at any time during the study.
  • Abnormal laboratory tests or clinically significant findings on safety tests conducted at the Screening Visit or at Check-in.
  • Confirmed or suspected infection with COVID-19 at the Screening Visit or Check-in.
  • Positive serology for human immunodeficiency virus (HIV) 1, HIV 2, or hepatitis B surface antigen (HBsAg), or positive for anti-HIV 1, anti-HIV 2, or anti hepatitis C virus (HCV) antibodies at the Screening Visit.
  • History of alcohol or drug addiction during the year before the Screening Visit, or has a positive drug or alcohol screen at the Screening Visit or Check-in.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05188261). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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