Overview
COMPARISON OF A NEW FORMULATION OF GOSERELIN (Pepti 3.6 mg) to Zoladex® 3.6 mg
Status:
Completed
Completed
Trial end date:
2020-06-07
2020-06-07
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The comparator drug (Zoladex 3.6 mg) is approved for use as a thinning agent for the endometrium prior to endometrial ablation. The dosing recommendation is one or two depots with each depot given four weeks apart. When two depots are administered, surgery should be performed within two to four weeks following administration of the second depot.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Peptigroupe Inc.Treatments:
Goserelin
Criteria
Inclusion Criteria:1. Be pre-Menopausal females with regular menstrual cycles and > 30 years of age 2.
Premenopausal at enrollment as determined by FSH measurement ≤ 60 IU/mL. 3. Endometrial
thickness at pre-treatment less than 20 mm. 4. Diagnosis of Dysfunctional Uterine Bleeding
and requiring endometrial ablation 5. Tumour negative cytology and histology 6. Appropriate
sized uterus with no anatomic pathologies 7. Patient is not pregnant and does not wish to
become pregnant in the future 8. Patient is willing to use a non-hormonal contraception
method during the study, nor an intra-uterine device 9. Patient has no endocrine disorders,
is not receiving hormonal therapies or non-steroidal anti-inflammatory medication.
(prophylactic antibiotics can be administered according to the usual practice of the
investigator) 10. Have the ability to understand the requirements of the study and is
willing to provide written informed consent 11. Agree to abide by the study restrictions
and return for the required assessments 12. Only patients which can be discontinued safely
from contra-indicated medications discussed below in section 7.4 can be included in the
study.
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Exclusion Criteria:
1. Be pregnant or have desire to conceive
2. Have abnormal endometrial cytology as confirmed by histology
3. Have active endometritis
4. Have active pelvic inflammatory disease
5. Have active sexually transmitted disease (STD), at the time of ablation. Note:
Treatment of STD documented in the chart serves as sufficient evidence of infection
resolution. Patient may be considered for study enrollment.
6. Presence of bacteremia, sepsis, or other active systemic infection
7. Have active infection of the genitals, vagina, cervix, uterus or urinary tract at the
time of inclusion
8. Known/suspected gynecological malignancy within the past 5 years
9. Known clotting defects or bleeding disorders
10. Untreated/unevaluated cervical dysplasia
11. Known/suspected abdominal/pelvic cancer
12. Atypical Hyperplasia
13. Prior uterine surgery (except low segment cesarean section) that interrupts the
integrity of the uterine wall (e.g., myomectomy or classical cesarean section
14. Currently on medications that could thin the myometrial muscle, such as long-term
steroid use (except inhaler or nasal therapy for asthma)
15. Currently on anticoagulants
16. Have a known hypersensitivity to gonadotropin releasing hormone (GnRH), GnRH agonists,
any LHRH agonists (e.g., leuprolide (Lupron®), goserelin ( Zoladex®) etc.) or to the
PLGA polymers contained in the study formulation
17. Have a severe liver disease (e.g., cirrhosis, chronic active hepatitis or chronic
persistent hepatitis) or has persistent ALT, AST ˃ 2 X ULN, serum creatinine ˃ 2 X
ULN, serum bilirubin ˃ 2 X ULN
18. Have received an investigational drug or participated in a clinical trial within the
last 30 days
19. Have clinically serious and/or unstable concurrent infection, medical illnesses or
conditions that are uncontrolled or whose control, in the opinion of the Investigator,
may be jeopardized by participation in this study or by the complications of this
therapy
20. Patients with BMI ˂ 18
21. Anticoagulated patients with INR ≥ 2
22. Patients with a history of QT prolongation, congenital long QT syndrome, electrolyte
abnormalities, CHF, or concurrent administration with QT prolonging drugs or QTc ˃450
msec.
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