A Dose Escalating Study to Assess the Safety and Tolerability of GT-001

NCT ID: NCT03490786

Last Updated: 2018-04-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-07-16
• Study Completion Date: 2017-10-02

Brief Summary

Dose escalation study of GT-001

Detailed Description

This is a dose-escalation design trial. Twelve evaluable subjects (n=12) with BMIs of 30 to 40 kg/m2 will receive a single dose of placebo followed by study drug applied directly to the surface of the tongue mucosa with a disposable pipette followed by a one-day washout. A total of seven (7) doses will escalate to a dose of 2.5 mg.

Conditions

Feeding and Eating Disorders

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Dose escalation

Single arm dose escalation.

Group Type: EXPERIMENTAL

GT-001

Intervention Type: DRUG

PK, PD Study to Determine Safety of Escalating Doses of GT-001

Interventions

GT-001

PK, PD Study to Determine Safety of Escalating Doses of GT-001

Intervention Type: DRUG

Other Intervention Names

PYY(3-36); Peptide YY (3-36)

Eligibility Criteria

Inclusion Criteria

• Adult participants with obesity class I and II (BMI 30-40 kg/m2)
• Willing and able to provide written informed consent after reviewing the design and risks of the study and prior to completing any study-related procedure
• Willing and able to understand and comply with all study procedures and requirements.
• Women must have a predictable menstrual cycle and taking either monophasic oral contraceptives, or transdermal (Ortho Evra and Evra) at least one month prior to the study.
• Alternatively, post-menopausal women (defined as period of spontaneous amenorrhea for more than 1 year), and bilateral oophorectomized women are allowed into the study.
• Must be able to complete the Weight Efficacy Life-Style Questionnaire (WEL).
• Systolic blood pressure 100-160 mmHg at the time of screening.
• Stable and compliant treatment with oral medications for at least 4 weeks prior to screening.
• Women of child bearing potential (WOCBP) and males must agree to use at least two forms of contraception, of which one includes a barrier method (male condom) by the male partner, during study participation and continued for at least 90 days after the conclusion of the final dose.
• In addition, sperm donations by male subjects are not permitted during the subject's participation in the research study and for at least 90 days after the conclusion of the final dose. This criterion may be waived for male subjects who have undergone a vasectomy at least 6 months prior to screening.
• Willing and able to abstain from drugs, , and tobacco during study participation.
• Must have abstained from alcohol use for 48 hours prior to study day 1 through the duration of the study
• Must have abstained from any tobacco- or nicotine-containing products (e.g., cigarettes, e-cigarettes, pipes, cigars, chewing tobacco, nicotine patches, nicotine lozenges, or nicotine gum) within 6 months prior to study day 1.
• History of stable weight for at least 3 months prior to study entry.

Exclusion Criteria

• Known hypersensitivity or allergy to Peptide YY, Pancreatic polypeptide (PP), other similar polypeptides or related compounds
• Known mutation to PYY or Y2 receptor gene (i.e., Pima Indians)
• Any medical condition for which modification of the medication that cannot be performed either safely or feasibly. Chronic diseases including metabolic, psychiatric, cardiovascular, endocrine, etc. for which the participant is not stable for 60 days prior to study initiation
• Female subjects who are pregnant or breast-feeding
• Female subjects of child bearing potential who are not on oral contraceptives or using biphasic or triphasic oral contraceptives
• Post-menopausal women who have not had a period of spontaneous amenorrhea for more than 1 year Unstable psychological or behavior profile (e.g., anxiety, depression)
• Subjects with fasting glucose levels greater than 125 mg/dl.
• Type I or Type II diabetes
• Poor dentition or oral pathology
• Unable or unwilling to give written informed consent.
• Temperature > 38°C (oral or equivalent)
• Sepsis or active infection requiring IV antimicrobial treatment
• Acute myocarditis or hypertrophic obstructive, restrictive, or constrictive cardiomyopathy (not including restrictive mitral filling patterns)
• Major neurologic event, including cerebrovascular events within 60 days prior to study initiation
• Significant pulmonary disease (e.g., history of oral daily steroid dependency, history of CO2 retention or need for intubation for acute exacerbation, or currently receiving IV steroids)
• Known hepatic impairment as indicated by any of the following:

• Total bilirubin > 3 mg/dl
• Albumin < 2.8 mg/dl, with other signs or symptoms of hepatic dysfunction
• Increased ammonia levels, if performed, with other signs or symptoms of hepatic dysfunction
• Any organ transplant recipient or currently listed (anticipated in the next 60 days) for transplant
• Major surgery within 30 days prior to study initiation
• Positive screen for Hepatitis B (HbsAg, Hepatitis B Surface Antigen), Hepatitis C (anti-HCV, Hepatitis C Antibody), or HIV (anti-HIV 1/2)
• Received an investigational intervention within 30 days prior to study initiation, or have received PYY3-36, GLP-1 agonists, insulin or DPP-IV inhibitors in a previous clinical trial.
• Consumption of alcohol within 48 hours prior to study day1 and through study day 15 or early termination
• Use of any tobacco- or nicotine-containing products (e.g., cigarettes, e-cigarettes, pipes, cigars, chewing tobacco, nicotine patches, nicotine lozenges, or nicotine gum) within 6 months
• A positive urine drug screen for ethanol, cotinine, cocaine, THC, barbiturates, amphetamines, benzodiazepines, and/or opiates
• A history of difficulty with donating blood, or having donated blood or blood products within 45 days prior to study initiation
• Use of weight loss drugs Orlistat (Alli or Xenical), Qsymia, Phentermine, Contrave, Lorcaserin, liraglutide, topiramate or exenatide within the last six months.
• Concurrent use of antihistamines
• Any condition that, in the opinion of the Investigator or Medical Monitor, would render the subject unsuitable for participation in the study
• Unable to consume the test meal

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Gila Therapeutics, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Orange County Research Center

Tustin, California, United States

Countries

United States

Other Identifiers

001

Identifier Type: -

Identifier Source: org_study_id