ClinicalTrials.Veeva

Menu

XW014 in Healthy Subjects and Patients With Type 2 Diabetes Mellitus (T2DM)

S

Sciwind Biosciences

Status and phase

Enrolling
Phase 1

Conditions

Type 2 Diabetes Mellitus

Treatments

Drug: Placebo
Drug: XW014

Study type

Interventional

Funder types

Industry

Identifiers

NCT05579314
XW014-001

Details and patient eligibility

About

This is a Phase 1, randomized, double-blind, placebo-controlled, first-in-human (FIH) study to evaluate the safety, tolerability, food effect (FE), pharmacokinetics (PK), and pharmacodynamics (PD) of orally administered XW014 in healthy participants and patients with T2DM. This study will consist of 4 parts: a Single Ascending Dose (SAD) part in healthy subjects (Part A), and Multiple Ascending Dose (MAD) parts in healthy subjects with elevated BMI (Part B and Part B-EXT) and patients with T2DM [Optional] (Part C).

Full description

Part A - SAD, including FE cohort: Healthy participants with BMI in the range of ≥18.5 kg/m2 to ≤35.0 kg/m2 will be randomized to receive a single oral dose of either XW014 or placebo in each of the planned SAD cohorts.

Part B and Part B-EXT - MAD in healthy participants with elevated BMI: Healthy subjects with BMI in the range of ≥30 kg/m2 to ≤40.0 kg/m2 will be randomized to receive oral doses of XW014 or placebo in each of the planned MAD cohorts.

Part C - MAD in patients with T2DM: Patients with T2DM for at least 6 months, having hemoglobin A1c (HbA1c) in the range of 6.5% to 8.5% will be randomized to receive oral doses of XW014 or placebo in each of the planned MAD cohorts.

Enrollment

152 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Ability and willingness to participate in the study, give written informed consent, and comply with the study restrictions and all protocol procedures

  2. Sex: male or female

  3. Weight: >50 kg, inclusive, at screening

  4. Age:

    1. For Part A 18 to 70 years, inclusive, at screening
    2. For Part B, Part B-EXT, and C 18 to 55 years, inclusive, at screening
  5. Body Mass Index

    1. For Part A: ≥18.5 kg/m2 and ≤35.0 kg/m2, inclusive, at screening
    2. For Part B and Part B-EXT: ≥30.0 kg/m2 and ≤40.0 kg/m2, inclusive, at screening
    3. For Part C: ≥25.0 kg/m2 and ≤40.0 kg/m2, inclusive, at screening
  6. Patients with T2DM for at least 6 months, having HbA1c of 6.5% to 8.5% (Part C)

Key Exclusion Criteria:

  1. History or clinically significant active disease of the gastrointestinal, cardiovascular, hepatic, neurologic, renal, pancreatic, immunologic, dermatologic, endocrine, genitourinary, or hematologic system
  2. Uncontrolled hypertension
  3. History of type 1 diabetes mellitus
  4. History or current diagnosis of acute or chronic pancreatitis or factors for pancreatitis
  5. Personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2 or subjects with suspected medullary thyroid carcinoma
  6. Existence of any surgical or medical condition that, in the judgment of the Investigator, might interfere with the absorption, distribution, metabolism, or excretion of the investigational product

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Sequential Assignment

Masking

Double Blind

152 participants in 8 patient groups, including a placebo group

SAD Cohort A - XW014
Active Comparator group
Description:
Single oral XW014 administration
Treatment:
Drug: XW014
Drug: XW014
SAD Cohort A - Placebo
Placebo Comparator group
Description:
Single oral placebo administration
Treatment:
Drug: Placebo
Drug: Placebo
MAD Cohort B - XW014
Active Comparator group
Description:
MAD in Healthy Subjects with Elevated BMI
Treatment:
Drug: XW014
Drug: XW014
MAD Cohort B - Placebo
Placebo Comparator group
Description:
MAD in Healthy Subjects with Elevated BMI
Treatment:
Drug: Placebo
Drug: Placebo
MAD Cohort C - XW014
Active Comparator group
Description:
MAD in Patients with T2DM
Treatment:
Drug: XW014
Drug: XW014
MAD Cohort C - Placebo
Placebo Comparator group
Description:
MAD in Patients with T2DM
Treatment:
Drug: Placebo
Drug: Placebo
MAD Cohort B-EXT - XW014
Active Comparator group
Description:
MAD in Healthy Subjects with Elevated BMI
Treatment:
Drug: XW014
Drug: XW014
MAD Cohort B-EXT - Placebo
Active Comparator group
Description:
MAD in Healthy Subjects with Elevated BMI
Treatment:
Drug: Placebo
Drug: Placebo

Trial contacts and locations

3

Loading...

Central trial contact

Eric Adegbite

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems