A Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With BPH

NCT ID: NCT02855892

Last Updated: 2022-03-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 161 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2016-10-31

Brief Summary

This clinical trial is designed as a randomized, placebo-controlled, single-blind, parallel design, multi-center, phase 2 clinical trial to evaluate the efficacy and safety of GV1001 in patients with benign prostatic hyperplasia. Eligible subjects are randomized into a group out of the three study groups and a placebo group after four weeks of placebo run-in period. Placebo run-in period is concurrently proceeded as a wash-out period for previous treatment of benign prostatic hyperplasia, and a placebo is administered intradermally twice with two-week interval during this period. After that, the randomized subjects receive a study drug and a placebo intradermally seven times with two-week interval by visiting at Week 0, 2, 4, 6, 8, 10, and 12. After the treatment period, the subjects additionally visit at Week 13 and 16, and the efficacy is evaluated at Week 4, 8, 12, 13, and 16, and the safety is evaluated over the 16-week period.

Detailed Description

Patients will be randomized equally between the four arms.

1. Control group (placebo, two-week interval): 38 subjects

2. Study group 1 (GV1001 0.4 mg, intradermal administration, two-week interval): 38 subjects

3. Study group 2 (GV1001 0.56 mg, intradermal administration, two-week interval): 38 subjects

4. Study group 3 (GV1001 0.56 mg, intradermal administration, four-week interval): 38 subjects

Conditions

Benign Prostatic Hyperplasia (BPH)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Control Group

\- Placebo, two-week interval, intradermal administration

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Study Group 1

\- GV1001 0.4 mg, two-week interval, intradermal administration

Group Type: EXPERIMENTAL

GV1001

Intervention Type: DRUG

Study Group 2

\- GV1001 0.56 mg, two-week interval, intradermal administration

Group Type: EXPERIMENTAL

GV1001

Intervention Type: DRUG

Study Group 3

• GV1001 0.56 mg, four-week interval, intradermal administration

: Should be visited every two weeks (GV1001 0.56 mg or placebo is administered alternately at every visit.)

Group Type: EXPERIMENTAL

Placebo

Intervention Type: OTHER

GV1001

Intervention Type: DRUG

Interventions

Placebo

Intervention Type: OTHER

GV1001

Intervention Type: DRUG

Other Intervention Names

Normal Saline 0.9 %; Tertomotide

Eligibility Criteria

Inclusion Criteria

All of the following criteria should be satisfied to be enrolled in this clinical trial.

1. A male at 50 years of age and older

2. A patient who satisfies the following clinical signs and symptoms of benign prostatic hyperplasia

① A patient with a volume of prostate gland (TRUS) > 30 cc

② A patient with moderate to severe lower urinary tract symptoms with IPSS ≥ 13

③ A patient with 5-15 mL/sec of maximum flow rate (Qmax) measured when urine volume was at least 125 mL

3. A patient with PSA level < 10 ng/mL (however, if 4 ng/mL < PSA < 10 ng/mL, a person with a biopsy result, confirming that he does not have prostate cancer)

4. A patient with residual urine volume ≤ 200 mL

5. A patient with intention of not using drugs which may affect benign prostatic hyperplasia (5-alpha reductase inhibitors, drugs similar to LHRH, alpha blockers, alpha-beta blockers, anticholinergics, antidiuretic hormones, diuretics, PDE-5 inhibitors, beta-3 adrenoceptor antagonists, etc.), drugs affecting immune system (steroids, immunosuppressants), or health functional foods which may affect a prostate gland (saw palmetto, etc.) during the clinical trial period

6. A patient has to consent not to participate in other clinical trials as a subject during this clinical trial period.

7. Before enrollment to the study, a patient has to consent to avoid pregnancy by using condoms for 90 days after the end of study participation period and treatment. (However, this is not applied if the patient had vasectomy.) Also, a partner of the patient has to consent to avoid pregnancy by using contraceptive devices or oral contraceptives during the patient's participation in clinical trial and for 90 days after the end of treatment, except if the partner reaches menopause or is surgically sterilized. (Consent should be obtained before visit 4, when necessary.)

1. A patient who satisfies the following clinical signs and symptoms of benign prostatic hyperplasia

① A patient with a volume of prostate gland (TRUS) > 30 cc *

② A patient with moderate to severe lower urinary tract symptoms with IPSS ≥ 13

③ A patient with 5-15 mL/sec of maximum flow rate (Qmax) measured when urine volume was at least 125 mL

2. A patient with residual urine volume ≤ 200 mL

3. A partner of the patient has to consent to avoid pregnancy by using contraceptive devices or oral contraceptives during the patient's participation in clinical trial and for 90 days after the end of treatment, except if the partner reaches menopause or is surgically sterilized.

(* In case that additional TRUS examination has been performed after screening, a decision should be made based on the latest result.)

Exclusion Criteria

If any one of the following is applied, a patient cannot be enrolled in this clinical trial.

1. A patient who has hypersensitivity reactions to ingredients of this drug.

2. A patient who received 5-alpha reductase inhibitors other than a drug used in this clinical trial before randomization (within six months)

3. A patient who received drugs similar to LHRH other than a drug used in this clinical trial

4. A patient who has received an unapproved study drug in the past or the study drug for this clinical trial (One exception: a patient can be enrolled when the drug is considered by an investigator not to affect prostate and urinary function, and the patient is not participating in other ongoing clinical trial.)

5. If diagnosed with prostate cancer in the past or at present

6. A patient who was considered by an investigator to have an influence to an evaluation on urine flow symptoms due to other previous or current diseases besides benign prostatic hyperplasia (e.g., neurogenic bladder, bladder neck contracture, urethral stricture, bladder cancer, malignant tumor in lower urinary tract, etc.)

7. A patient who had surgeries or radiation therapies for prostate gland, bladder or pelvis, or who had invasive treatments for benign prostatic hyperplasia

8. A patient who has severe medical condition which may be cause problem to conduct the clinical trial (e.g., chronic heart failure (CHF), difficult-to-control diabetes (HbA1c > 7%), mental disorder, drug, or alcohol abuse, etc.)

9. A patient with moderate to severe liver hypofunction and severe kidney hypofunction (less than 30 mL/min of creatinine clearance)

10. A patient who receives drugs affecting immune system (e.g., immunosuppressives, steroids for systemic action, etc.)

11. Any other patients who are considered to be ineligible for this study by an investigator

• Minimum Eligible Age: 50 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

GemVax & Kael

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kyung Seop Lee

Role: STUDY_CHAIR

Department of Urology, Dongguk University Gyeongju Hospital

Locations

Hanyang University Guri Hospital

Guri-si, Gyeonggi-do, South Korea

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea

Dongguk University Gyeongju Hospital

Gyeongju, Gyeongsangbuk-do, South Korea

Inje University Busan Paik Hospital

Busan, , South Korea

Keimyung University Dongsan Medical Center

Daegu, , South Korea

Chung-ang University Hospital

Seoul, , South Korea

Eulji General Hospital

Seoul, , South Korea

Severance Hospital

Seoul, , South Korea

Countries

South Korea

Other Identifiers

KG 3/2014

Identifier Type: -

Identifier Source: org_study_id