Benign Prostatic Hyperplasia (BPH)Phase 2NCT02855892
A Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With BPH
A Phase 2 study testing GV1001 in people with Benign Prostatic Hyperplasia (BPH), run by GemVax & Kael at 8 sites in South Korea.
Trial 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. Read more about this study
- Who is it for?
- Ages 50 years and older, men only
- Conditions the study is for
- Benign Prostatic Hyperplasia (BPH)
- What is being tested?
- GV1001
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 161 participants
- Where
- 8 sitesSouth Korea
- Study dates
- Oct 2015to Oct 2016
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 50 years and older
- Men only
- No healthy volunteers
- Adult, Older adult
[Inclusion Criteria]
All of the following criteria should be satisfied to be enrolled in this clinical trial.
- A male at 50 years of age and older
- 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
- 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)
- A patient with residual urine volume ≤ 200 mL
- 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
- A patient has to consent not to participate in other clinical trials as a subject during this clinical trial period.
- 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.)
[Exclusion Criteria]
If any one of the following is applied, a patient cannot be enrolled in this clinical trial.
- A patient who has hypersensitivity reactions to ingredients of this drug.
- A patient who received 5-alpha reductase inhibitors other than a drug used in this clinical trial before randomization (within six months)
- A patient who received drugs similar to LHRH other than a drug used in this clinical trial
- 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.)
- If diagnosed with prostate cancer in the past or at present
- 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.)
- A patient who had surgeries or radiation therapies for prostate gland, bladder or pelvis, or who had invasive treatments for benign prostatic hyperplasia
- 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.)
- A patient with moderate to severe liver hypofunction and severe kidney hypofunction (less than 30 mL/min of creatinine clearance)
- A patient who receives drugs affecting immune system (e.g., immunosuppressives, steroids for systemic action, etc.)
- Any other patients who are considered to be ineligible for this study by an investigator
[Inclusion Criteria for Randomization]
- 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
- A patient with residual urine volume ≤ 200 mL
- 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.)
Trial locations and contacts
8 sites in 1 country.
8 sites in 1 country
South Korea8 sites
Inje University Busan Paik Hospital
Busan
Keimyung University Dongsan Medical Center
Daegu
Hanyang University Guri Hospital
Guri-si, Gyeonggi-do
Dongguk University Gyeongju Hospital
Gyeongju, Gyeongsangbuk-do
Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do
Chung-ang University Hospital
Seoul
Eulji General Hospital
Seoul
Severance Hospital
Seoul
About this study
Official title: A Randomized, Placebo-controlled, Single-blind, Parallel Design, Multi-center, Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With Benign Prostatic Hyperplasia (BPH)
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.
Read the detailed description
Patients will be randomized equally between the four arms.
- Control group (placebo, two-week interval): 38 subjects
- Study group 1 (GV1001 0.4 mg, intradermal administration, two-week interval): 38 subjects
- Study group 2 (GV1001 0.56 mg, intradermal administration, two-week interval): 38 subjects
- Study group 3 (GV1001 0.56 mg, intradermal administration, four-week interval): 38 subjects
- Conditions
- Benign Prostatic Hyperplasia (BPH)
- Being tested
- Placebo, GV1001
- Keywords
- GV1001, BPH, Benign prostatic hyperplasia
- Medical subject headings
- Prostatic Hyperplasia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PlaceboOther
Also called Normal Saline 0.9 %
GV1001Drug
Also called Tertomotide
| Study group | Role | What they receive |
|---|---|---|
| Control Group | Placebo comparator | - Placebo, two-week interval, intradermal administration Receives: Other: Placebo |
| Study Group 1 | Experimental | - GV1001 0.4 mg, two-week interval, intradermal administration Receives: Drug: GV1001 |
| Study Group 2 | Experimental | - GV1001 0.56 mg, two-week interval, intradermal administration Receives: Drug: GV1001 |
| Study Group 3 | Experimental | - 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.) Receives: Other: Placebo; Drug: GV1001 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Evaluation of doses of GV1001 by comparing the level of change in IPSS scores in three study groups to a control group.
IPSS questionnaire: 7-item questionnaire that measures urinary symptoms, but with an additional, independent eighth question on quality of life. It measures the level of urinary symptoms (including incomplete emptying, frequency, intermittency, urgency, weak stream, straining, and nocturia) reported as the total IPSS score. The first 7 items has a 6-point response scale (0=none/never to 5=almost always/5 or more times) with a total score that can range from 0-35: mild (0-7), moderate (8-19), or severe (20-35). The last item assesses quality of life reported as a Quality of Life assessment index.
Measured: at Week 0, 4, 8, 12, 13, and 16
Secondary outcomes (6)
Change in volume of prostate gland (TRUS) compared to the baseline
The amount of change from Transrectal Ultrasonography(TRUS) compared to the baseline
Measured: at screening and Week 16
Change in maximum flow rate (Qmax) compared to the baseline
The amount of change from Maximum(peak) Urinary Flow Rate compared to the baseline
Measured: at Week 0, 4, 8, 12, 13, and 16
Change in International Index of Erectile Function (IIEF) compared to the baseline
IIEF questionnaire: 15-item, 5 domain scale collected by subject interview, relating to the subjects' experience of erectile function (and other sexual parameters) over the previous 4 weeks.
Measured: at Week 0, 4, 8, 12, 13, and 16
Change in prostate-specific antigen (PSA) compared to the baseline
The amount of change from Prostate-specific Antigen (PSA) compared to the baseline
Measured: at Week 0, 13, and 16
Change in residual urine volume compared to the baseline
The amount of change from Residual Urine Volume compared to the baseline
Measured: at Week 0, 4, 8, 12, 13, and 16
Change in hormones (testosterone, DHT) compared to the baseline
The amount of change from Hormones (Testosterone, DHT) compared to the baseline
Measured: at Week 0, 4, 8, 12, 13, and 16
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Aug 2016 (estimated)
- Study startOct 2015
- Primary completionOct 2016
- Study completionOct 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Benign Prostatic Hyperplasia (BPH)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 161 participants (actual)
Sponsor and investigators
- Lead sponsor
- GemVax & Kael
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Kyung Seop Lee, Study chair, Department of Urology, Dongguk University Gyeongju Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02855892
- Sponsor's protocol ID
- KG 3/2014
- Status last verified
- Feb 2022
- First submitted
- 1 Aug 2016
- Last updated
- 4 Mar 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Mar 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Placebo-controlled, Single-blind, Parallel Design, Multi-center, Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With Benign Prostatic Hyperplasia (BPH)
- ClinicalTrials.gov ID
- NCT02855892
- Acronym / sponsor ID
- KG 3/2014
- Conditions
- Benign Prostatic Hyperplasia (BPH)
- Keywords
- GV1001, BPH, Benign prostatic hyperplasia
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 161 participants (actual)
- Lead sponsor
- GemVax & KaelIndustry (pharma, biotech, devices)
- Study start
- Oct 2015
- Primary completion
- Oct 2016 (actual)
- Study completion
- Oct 2016 (actual)
- First posted
- 4 Aug 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
- Control group (placebo, two-week interval): 38 subjects
- Study group 1 (GV1001 0.4 mg, intradermal administration, two-week interval): 38 subjects
- Study group 2 (GV1001 0.56 mg, intradermal administration, two-week interval): 38 subjects
- Study group 3 (GV1001 0.56 mg, intradermal administration, four-week interval): 38 subjects
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Control Group | Placebo comparator | Other: Placebo- Placebo, two-week interval, intradermal administration |
| Study Group 1 | Experimental | Drug: GV1001- GV1001 0.4 mg, two-week interval, intradermal administration |
| Study Group 2 | Experimental | Drug: GV1001- GV1001 0.56 mg, two-week interval, intradermal administration |
| Study Group 3 | Experimental | Other: Placebo, Drug: GV1001- 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.) |
Who may qualify
- Ages
- 50 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PlaceboAlso: Normal Saline 0.9 % | Other | Control Group, Study Group 3 |
| GV1001Also: Tertomotide | Drug | Study Group 1, Study Group 2, Study Group 3 |
Primary outcome
Evaluation of doses of GV1001 by comparing the level of change in IPSS scores in three study groups to a control group.
Time frame: at Week 0, 4, 8, 12, 13, and 16
IPSS questionnaire: 7-item questionnaire that measures urinary symptoms, but with an additional, independent eighth question on quality of life. It measures the level of urinary symptoms (including incomplete emptying, frequency, intermittency, urgency, weak stream, straining, and nocturia) reported as the total IPSS score. The first 7 items has a 6-point response scale (0=none/never to 5=almost always/5 or more times) with a total score that can range from 0-35: mild (0-7), moderate (8-19), or severe (20-35). The last item assesses quality of life reported as a Quality of Life assessment index.
6 secondary outcomes
Change in volume of prostate gland (TRUS) compared to the baseline
Time frame: at screening and Week 16
Change in maximum flow rate (Qmax) compared to the baseline
Time frame: at Week 0, 4, 8, 12, 13, and 16
Change in International Index of Erectile Function (IIEF) compared to the baseline
Time frame: at Week 0, 4, 8, 12, 13, and 16
Change in prostate-specific antigen (PSA) compared to the baseline
Time frame: at Week 0, 13, and 16
Change in residual urine volume compared to the baseline
Time frame: at Week 0, 4, 8, 12, 13, and 16
Change in hormones (testosterone, DHT) compared to the baseline
Time frame: at Week 0, 4, 8, 12, 13, and 16
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Mar 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kyung Seop Lee study chair
Department of Urology, Dongguk University Gyeongju Hospital
8 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing GV1001 in people with Benign Prostatic Hyperplasia (BPH), run by GemVax & Kael at 8 sites in South Korea.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 8 sites in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Evaluation of doses of GV1001 by comparing the level of change in IPSS scores in three study groups to a control group. (time frame: at Week 0, 4, 8, 12, 13, and 16). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Mar 2022.