To Determine an Effective Dose of VERU-100 for the Treatment of Advanced Prostate Cancer

NCT ID: NCT04843319

Last Updated: 2023-05-19

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-09
• Study Completion Date: 2023-01-19

Brief Summary

To determine an effective dose of VERU-100 for the treatment of advanced prostate cancer by assessing its effect on testosterone levels by Day 28 and maintenance through Day 91.

Detailed Description

This study is a multicenter, randomized, open-label, dose finding study of VERU-100 to attain and maintain serum total testosterone levels within castrate range (<50ng/dL) in men with advanced prostate cancer. Stage 1 of the study will assess the effect of VERU-100 at various doses. Stage 2 will further assess the efficacy of the effective doses of VERU-100 in an expanded patient population.

Conditions

Advanced Prostate Adenocarcinoma

Study Design

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

Study Groups

VERU-100 at various doses

2 ml, 2.5 ml, 3 ml, 3.5 ml of VERU-100

Group Type: EXPERIMENTAL

VERU-100

Intervention Type: DRUG

GnRH antagonist

Interventions

VERU-100

GnRH antagonist

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Be over 18 years of age
• Be able to communicate effectively with the study personnel
• Have histologically confirmed prostate cancer
• Have prostate cancer staged T3-4NxMx or TxN1Mx or TxNxM1 according to the TNM classification or the patient should have rising PSA after failed local therapy and be candidate for androgen deprivation therapy
• Have a QTc interval <440 ms
• Subjects are judged by the attending physician and/or Principal Investigator to be a candidate for androgen deprivation therapy (continuous therapy)
• ECOG performance status of 0 to 2
• Baseline morning serum testosterone levels >150 ng/dL at Screening Visit
• Have a life expectancy of ≥18 months
• Subjects must agree to use acceptable methods of contraception

1. If their female partners are pregnant or lactating, acceptable methods of contraception from the time of the first administration of study medication until 6months following administration of the last dose of study medication must be used. Acceptable methods are: Condom used with spermicidal foam/gel/film/cream/suppository. If the subject has undergone surgical sterilization (vasectomy with documentation of azoospermia),a condom with spermicidal foam/gel/film/cream/suppository should be used.

2. If the male subject's partner could become pregnant, use acceptable methods of contraception from the time of the first administration of study medication until 6 months following administration of the last dose of study medication. Acceptable methods of contraception are as follows: Condom with spermicidal foam/gel/cream/suppository [i.e.,barrier method of contraception], surgical sterilization (vasectomy with documentation of azoospermia) and a barrier method {condom used with spermicidal foam/gel/film/cream/suppository}, the female partner uses oral contraceptives (combination estrogen/progesterone pills), injectable progesterone or subdermal implants and a barrier method (condom used with spermicidal foam/gel/film/cream/suppository).

3. If the female partner has undergone documented tubal ligation (female sterilization), a barrier method (condom used with spermicidal foam/gel/film/cream/suppository) should also be used.

4. If the female partner has undergone documented placement of an intrauterine device (IUD) or intrauterine system (IUS),a barrier method (condom with spermicidal foam/gel/film/cream/suppository) should also be used.

• Laboratory values within the following ranges: hemoglobin ≥10 gm/dL, total bilirubin

• 1.5x upper limit of normal (ULN), AST ≤2.5x ULN, ALT ≤2.5x ULN,
• 1.5 mg/dL, absolute neutrophil count ≥1500 cell/uL and platelets ≥100,000 cells/uL.
• Creatinine clearance ≥60 mL/min based on Cockcroft-Gault equation.
• Subject is willing to comply with the requirements of the protocol through the end of the study

Exclusion Criteria

• Prior androgen deprivation therapy within 6 months prior to Screening Visit.
• Potentially curable disease receiving ADT for localized disease
• History of bilateral orchiectomy, adrenalectomy, or hypophysectomy
• Received chemotherapy, cryotherapy, or antiandrogen therapy within 8 weeks prior to the Screening visit for the treatment of prostate cancer.
• Known hypersensitivity to cetrorelix or other LHRH antagonists
• History of Torsade de Pointes
• Currently taking QT-prolonging drugs
• Any disease or condition (medical or surgical) which might compromise the hematologic, cardiovascular, endocrine, pulmonary, renal, gastrointestinal, hepatic, or central nervous system; or other conditions that may interfere with the absorption, distribution, metabolism or excretion of study drug, or would place the subject at increased risk
• Use of exogenous testosterone within 6 months of Screening Visit
• Use of 5α-reductase inhibitor within 3 months of Screening Visit
• Use of systemic corticosteroids at a dose >10 mg/day at Screening
• Major surgery within 4 weeks of Screening Visit (including surgery for prostate cancer)
• Uncontrolled symptomatic congestive heart failure (NYHA Class III -IV), unstable angina pectoris, cardiac arrhythmia, or uncontrolled atrial fibrillation
• History of diabetes mellitus Type 1. Uncontrolled diabetes mellitus Type 2 (control with oral hypoglycemic agents are allowed)
• Received an investigational drug within a period of 90days prior to enrollment in the study
• Received the study medication (VERU-100) previously
• Have been previously diagnosed or treated for active cancer(other than prostate cancer or non-melanoma skin cancer) within the previous five years

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Veru Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bernette

Role: STUDY_CHAIR

Veru Inc.

Locations

Arizona Urology Specialist

Tucson, Arizona, United States

Urology Associates of Southern Arizona

Tucson, Arizona, United States

San Bernardino Urological Associates

San Bernardino, California, United States

Genesis Research, LLC

San Diego, California, United States

Debbie Urology Johnson

Jeffersonville, Indiana, United States

Chesapeake Urology Research Associates

Towson, Maryland, United States

Clinical Research Solutions

Middleburg Heights, Ohio, United States

MidLantic Urology

Bala-Cynwyd, Pennsylvania, United States

Carolina Urologic Research Center

Myrtle Beach, South Carolina, United States

Houston Metro Urology

Houston, Texas, United States

Urology San Antonio

San Antonio, Texas, United States

Countries

United States

Other Identifiers

V2010001

Identifier Type: -

Identifier Source: org_study_id