Overview

16-week Flexible vs. 8-week Semaglutide Titration

Status:
Recruiting
Trial end date:
2022-09-10
Target enrollment:
0
Participant gender:
All
Summary
Semaglutide is a Glucagon Like Peptide 1 (GLP-1) receptor agonist recently approved in Israel to improve glycemic control in patients with type 2 diabetes mellitus. Semaglutide is currently administered as a weekly subcutaneous injection.Treatment with semaglutide is associated with the occurrence of gastrointestinal adverse events (GI-AEs) commonly observed during GLP-1 receptor agonist treatment. The most common adverse reactions, reported in ≥5% of patients treated with semaglutide are nausea, vomiting, diarrhea, abdominal pain and constipation. In this trial we plan to explore the effect of a slower titration regimen of semaglutide vs. the current label-recommended dose escalation regimen on the occurrence of GI-AEs.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tel-Aviv Sourasky Medical Center
Criteria
Inclusion Criteria:

- Have personally signed and dated the informed consent form indicating that he/she has
been informed of all pertinent aspects of the trial.

- Be willing and able to comply with the scheduled visits and other study procedures.

- Meet one of the following categories:

1. The subject is a male.

2. The subject is a female who is not of reproductive potential, defined as a female
who either: (1) is postmenopausal (defined as at least 12 months with no menses
in women ≥45 years of age); (2) has had a hysterectomy and/or bilateral
oophorectomy, bilateral salpingectomy, or bilateral tubal ligation/occlusion at
least 6 weeks prior to screening; OR (3) has a congenital or acquired condition
that prevents childbearing.

3. The subject is a female who is of reproductive potential and agrees to avoid
becoming pregnant: while receiving study drug and for 60 days after the last dose
of study drug by complying with one of the following: (1) practice abstinence†
from heterosexual activity OR (2) use (or have her partner use) acceptable
contraception during heterosexual activity. Acceptable methods of contraception
are‡:

Single method (one of the following is acceptable):

- non-hormonal intrauterine device (IUD)

- vasectomy of a female subject's male partner

Combination method (requires use of two of the following):

- diaphragm with spermicide (cannot be used in conjunction with cervical cap/spermicide)

- cervical cap with spermicide (nulliparous women only)

- contraceptive sponge (nulliparous women only)

- male condom or female condom (cannot be used together)

Exclusion Criteria:

- Has a known contraindication to use of GLP-1 agonists.

- Has been treated with a GLP-1 agonist in the last 30 days.

- Has a history of type 1 diabetes mellitus

- Has a medical history of untreated active proliferative retinopathy.

- Has other severe acute or chronic medical or psychiatric condition or laboratory
abnormality that may increase the risk associated with study participation or blinded
investigational product administration or may interfere with the interpretation of
study results and, in the judgment of the investigator, would make the subject
inappropriate for entry into this trial.