HealthyPhase 2NCT03455075
Study of Spermatogenesis Suppression With DMAU Alone or With LNG Versus Placebo Alone in Normal Men
A Phase 2 study testing Dimethandrolone-Undecanoate and Levonorgestrel 0.03 MG in people with Healthy and Men, run by Premier Research at 2 sites in United States.
Trial summary
This is a Phase IIa multicenter, double-blind, placebo-controlled study in healthy men to evaluate the spermatogenesis suppression after oral administration of Dimethandrolone Undecanoate (DMAU) alone or with Levonorgestrel (LNG) for 12 weeks versus placebo alone. Read more about this study
- Who is it for?
- Ages 18 to 50 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Healthy, Men, Male Contraception
- What is being tested?
- Dimethandrolone-Undecanoate and Levonorgestrel 0.03 MG
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 92 participants
- Where
- 2 sitesUnited States
- Study dates
- 16 Apr 2018to 5 Mar 2020
- 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 18 to 50 years
- Men only
- Healthy volunteers accepted
- Adult
Men who meet all the following criteria are eligible for enrollment in the trial:
- Male volunteers in good health as confirmed by physical examination, medical history, and clinical laboratory tests of blood and urine at the time of screening.
- 18 to 50 years of age (inclusive) at the time of the screening visit.
- BMI ≤36 calculated as weight in kg/ (height in m2).
- No history of steroid hormone use in the three months prior to the first screening visit or any current medication use which might interfere with steroid metabolism.
- Subject agrees to use a recognized effective method of contraception with any female partner (refer to Appendix 7 for acceptable forms of contraception) during the course of the study treatment and recovery phases until recovery is confirmed and study exit occurs.
- Subjects will refrain from donating blood or plasma during the study period and from participating in other investigational drug studies.
- Subjects will be advised to refrain from excessive alcoholic consumption during the study period. (No more than 15 drinks per week and no alcohol consumption within 24 hours of a study visit.)
- Subjects will be advised to refrain from excessive marijuana consumption during the study period. (No more than 3 uses per week and no consumption within 24 hours of a study visit.)
- No known or suspected current alcohol dependence syndrome, chronic marijuana use, or any illicit drug use that may affect metabolism/transformation of steroid hormones and study treatment compliance.
- Subjects will be advised to refrain/abstain from grapefruit juice during the study period.
- In the opinion of the investigator, subject is able to comply with the protocol, understand and sign an informed consent and HIPAA form.
- Subjects will be advised to refrain from major changes in their level of exercise during the study period.
Men who meet any of the following criteria are NOT eligible for enrollment in the trial:
- Men participating in another clinical trial involving an investigational drug within the 30 days prior to the first screening visit.
- Men not living in the catchment area of the clinic or within a reasonable distance from the study site.
- Clinically significant abnormal physical or laboratory findings at screening.
- Elevated PSA (levels ≥ 2.5 ng/mL) at screening, according to local laboratory normal values.
- IPSS score ≥ 10.
- Abnormal serum chemistry values at screening, according to local laboratory reference ranges that indicate liver or kidney dysfunction or that may be considered clinically significant. In addition, the following upper limits will be observed: fasting bilirubin less than 2 mg/dL, cholesterol less than 221 mg/dL, and fasting triglycerides less than 201 mg/dL.
- Abnormal semen analyses or abnormal semen concentration as defined by the WHO semen manual (< 15 million/mL).
- Use of androgens within 3 months before first screening visit except for long acting testosterone which requires a wash out period of 4 months prior to screening.
- Ongoing use of androgens or other compounds for body building including nutritional supplements.
- Systolic BP ≥130 mm Hg and Diastolic blood pressure BP ≥ 80 and mm Hg; Blood pressure (BP) will be taken 3 times at 5 - minute intervals and the mean of second and third measurements will be used to determine eligibility. (Note: Diagnosis of hypertension or treatment of hypertension is exclusionary.)
- PHQ-9 score of 15 or above.
- History of hypertension, including hypertension controlled with treatment.
- Known history of primary testicular disease or disorders of the hypothalamic-pituitary axis.
- Benign or malignant liver tumors; active liver disease.
- History of breast carcinoma.
- Known history of androgen deficiency due to hypothalamic-pituitary or testicular disease.
- Known history of cardiovascular, renal, hepatic or prostatic disease or significant psychiatric illness.
- Positive serology for active Hepatitis (not immunization-related serology) or HIV at screening visit.
- A serious systemic disease such as diabetes mellitus.
- History of known, untreated sleep apnea.
- Partner is known to be pregnant.
- Men desiring fertility within 12 months of signing consent for study participation.
- Men participating in competitive sports where drug screening for prohibited substances (including anabolic steroids) is routine. Exclusion is due to the potential of testing positive for androgens that may occur from their study participation coupled with the unknown efficacy (i.e. duration of positive testing) from 12-week daily use of DMAU.
- Use of sex steroids or medications which might interfere with steroid metabolism (i.e. ketoconazole, finasteride, oral corticosteroids, dutasteride and statins).
- Use of medications that will interfere or interact with DMAU or LNG.
- Known hypersensitivity to any of the active substances of DMAU, of the excipients of the study treatment, or LNG.
Trial locations and contacts
2 sites in 1 country.
United States2 sites
University of Washington Medical Center & Health Sciences
Seattle, Washington, 98195
Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center
Torrance, California, 90509
About this study
Official title: A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial of Spermatogenesis Suppression After Oral Administration of Dimethandrolone Undecanote (DMAU) Alone or With Levonorgestrel (LNG) for 12 Weeks Versus Placebo Alone in Normal Men
This is a Phase IIa multicenter, double-blind, placebo-controlled study in healthy men to evaluate the spermatogenesis suppression after oral administration of Dimethandrolone Undecanoate (DMAU) alone or with Levonorgestrel (LNG) for 12 weeks versus placebo alone.
Read the detailed description
This 12 week repeated dose study will be conducted at two centers: the Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center and the University of Washington. The sites propose to enroll approximately 100 men with a goal of enrolling 20 healthy male subjects in each of the 4 active groups and 20 in the placebo group for 12 weeks of treatment. The goal is to complete at least 17 efficacy evaluable subjects in each group. The DMAU for this study will be castor oil formulation administered after a 25 to 30 g fat meal. The oral dose of LNG will be 30 mcg per day. The study volunteers will be randomized to one of five treatment groups:
Group 1: Lower DMAU dose (100 mg per day) + LNG (30 mcg per day) (n=20) Group 2: Middle DMAU dose (200mg per day) + LNG (30 mcg per day) (n=20) Group 3: Middle DMAU dose (200 mg per day) + placebo LNG (n=20) Group 4: Higher DMAU dose (400 mg per day) + placebo LNG (n=20) Group 5: Placebo DMAU capsules and placebo LNG capsules (n=20)
Each treatment group will receive the identical number of capsules in blinded fashion so that each subject will receive an identical number of capsules in order to maintain the blind.
- Conditions
- Healthy, Men, Male Contraception
- Being tested
- Dimethandrolone-Undecanoate, Levonorgestrel 0.03 MG, Placebo oral capsule
- Keywords
- Healthy Men, Male Contraception, Androgen, Dimethandrolone, Levonorgestrel
- Medical subject headings
- Multiple Endocrine Neoplasia Type 1
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dimethandrolone-UndecanoateDrug
Also called DMAU
Single doses of DMAU in castor oil/benzyl benzoate administered in 100 mg capsules.
Levonorgestrel 0.03 MGDrug
Also called LNG
Single doses of LNG administered in 30 mcg capsules.
Placebo oral capsuleDrug
Placebo capsules that look like DMAU and LNG capsules but with no active ingredients.
| Study group | Role | What they receive |
|---|---|---|
| Lower DMAU + LNG | Experimental | DMAU 100 mg + LNG 30 mcg administered orally in capsules. Receives: Drug: Dimethandrolone-Undecanoate; Drug: Levonorgestrel 0.03 MG |
| Middle DMAU + LNG | Experimental | DMAU 200 mg + LNG 30 mcg administered orally in capsules. Receives: Drug: Dimethandrolone-Undecanoate; Drug: Levonorgestrel 0.03 MG |
| Middle DMAU + Placebo | Experimental | DMAU 200 mg + placebo administered orally in capsules. Receives: Drug: Dimethandrolone-Undecanoate; Drug: Placebo oral capsule |
| Higher DMAU + Placebo | Experimental | DMAU 400 mg + placebo administered orally in capsules. Receives: Drug: Dimethandrolone-Undecanoate; Drug: Placebo oral capsule |
| Placebo | Placebo comparator | Placebo administered orally capsules. Receives: Drug: Placebo oral capsule |
What is being measured
The primary outcome is the main question the study is designed to answer.
Suppression of spermatogenesis as assessed by semen analyses using number of subjects with sperm concentration <3 million (M)/mL with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Secondary outcomes (32)
Assessing suppression of gonadotropins using percentage of subjects with FSH and LH ≤ 1.0 IU/L.
Measured: 2 months
Changes from baseline in sperm concentration.
Measured: 4 - 6 months
Changes from baseline in LH level.
Measured: 4 - 6 months
Changes from baseline in FSH level.
Measured: 4 - 6 months
Changes from baseline in Testosterone level.
Measured: 4 - 6 months
Changes from baseline in Estradiol level.
Measured: 4 - 6 months
Changes from baseline in DHT level.
Measured: 4 - 6 months
Changes from baseline in SHBG level.
Measured: 4 - 6 months
Changes from baseline in DMA level.
Measured: 4 - 6 months
Changes from baseline in DMAU level.
Measured: 4 - 6 months
Changes from baseline in LNG level.
Measured: 4 - 6 months
Incidence of treatment emergent adverse events (safety and tolerability) with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in sodium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in potassium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in bicarbonate with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in chloride with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in fasting glucose with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in blood urea nitrogen with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in creatinine with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in calcium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in total bilirubin with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in alkaline phosphatase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in alanine aminotransferase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in aspartate transaminase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in albumin with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in PSA with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Measured: 12 weeks
Changes from baseline in sexual function with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the psychosexual daily questionnaire.
Measured: 12 weeks
Changes from baseline in prostate function with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the International Prostate Symptom Score.
Measured: 12 weeks
Changes from baseline in mood with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the Patient Health Questionnaire-9.
Measured: 12 weeks
Changes from baseline in blood pressure.
Measured: 4 - 6 months
Changes from baseline in heart rate.
Measured: 4 - 6 months
Changes from baseline in weight.
Measured: 4 - 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Mar 2018
- Study start16 Apr 2018
- Primary completion5 Mar 2020
- Study completion5 Mar 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HealthyStudies 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
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 92 participants (actual)
Sponsor and investigators
- Lead sponsor
- Premier Research
- Sponsor type
- University, hospital or other
- Collaborators
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, University of Washington
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03455075
- Sponsor's protocol ID
- CCN010B
- Status last verified
- Oct 2025
- First submitted
- 22 Feb 2018
- Last updated
- 30 Oct 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multicenter, Randomized, Placebo-Controlled, Double-Blind Trial of Spermatogenesis Suppression After Oral Administration of Dimethandrolone Undecanote (DMAU) Alone or With Levonorgestrel (LNG) for 12 Weeks Versus Placebo Alone in Normal Men
- ClinicalTrials.gov ID
- NCT03455075
- Acronym / sponsor ID
- CCN010B
- Conditions
- Healthy, Men, Male Contraception
- Keywords
- Healthy Men, Male Contraception, Androgen, Dimethandrolone, Levonorgestrel
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 92 participants (actual)
- Lead sponsor
- Premier ResearchUniversity, hospital or other
- Collaborators
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, University of Washington
- Study start
- 16 Apr 2018 (actual)
- Primary completion
- 5 Mar 2020 (actual)
- Study completion
- 5 Mar 2020 (actual)
- First posted
- 6 Mar 2018 (actual)
- 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 is a Phase IIa multicenter, double-blind, placebo-controlled study in healthy men to evaluate the spermatogenesis suppression after oral administration of Dimethandrolone Undecanoate (DMAU) alone or with Levonorgestrel (LNG) for 12 weeks versus placebo alone.
Detailed description
This 12 week repeated dose study will be conducted at two centers: the Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center and the University of Washington. The sites propose to enroll approximately 100 men with a goal of enrolling 20 healthy male subjects in each of the 4 active groups and 20 in the placebo group for 12 weeks of treatment. The goal is to complete at least 17 efficacy evaluable subjects in each group. The DMAU for this study will be castor oil formulation administered after a 25 to 30 g fat meal. The oral dose of LNG will be 30 mcg per day. The study volunteers will be randomized to one of five treatment groups:
Group 1: Lower DMAU dose (100 mg per day) + LNG (30 mcg per day) (n=20) Group 2: Middle DMAU dose (200mg per day) + LNG (30 mcg per day) (n=20) Group 3: Middle DMAU dose (200 mg per day) + placebo LNG (n=20) Group 4: Higher DMAU dose (400 mg per day) + placebo LNG (n=20) Group 5: Placebo DMAU capsules and placebo LNG capsules (n=20)
Each treatment group will receive the identical number of capsules in blinded fashion so that each subject will receive an identical number of capsules in order to maintain the blind.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 5
| Arm | Type | Receives |
|---|---|---|
| Lower DMAU + LNG | Experimental | Drug: Dimethandrolone-Undecanoate, Drug: Levonorgestrel 0.03 MGDMAU 100 mg + LNG 30 mcg administered orally in capsules. |
| Middle DMAU + LNG | Experimental | Drug: Dimethandrolone-Undecanoate, Drug: Levonorgestrel 0.03 MGDMAU 200 mg + LNG 30 mcg administered orally in capsules. |
| Middle DMAU + Placebo | Experimental | Drug: Dimethandrolone-Undecanoate, Drug: Placebo oral capsuleDMAU 200 mg + placebo administered orally in capsules. |
| Higher DMAU + Placebo | Experimental | Drug: Dimethandrolone-Undecanoate, Drug: Placebo oral capsuleDMAU 400 mg + placebo administered orally in capsules. |
| Placebo | Placebo comparator | Drug: Placebo oral capsulePlacebo administered orally capsules. |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- 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 |
|---|---|---|
| Dimethandrolone-UndecanoateAlso: DMAUSingle doses of DMAU in castor oil/benzyl benzoate administered in 100 mg capsules. | Drug | Higher DMAU + Placebo, Lower DMAU + LNG, Middle DMAU + LNG, Middle DMAU + Placebo |
| Levonorgestrel 0.03 MGAlso: LNGSingle doses of LNG administered in 30 mcg capsules. | Drug | Lower DMAU + LNG, Middle DMAU + LNG |
| Placebo oral capsulePlacebo capsules that look like DMAU and LNG capsules but with no active ingredients. | Drug | Higher DMAU + Placebo, Middle DMAU + Placebo, Placebo |
Primary outcome
Suppression of spermatogenesis as assessed by semen analyses using number of subjects with sperm concentration <3 million (M)/mL with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
32 secondary outcomes
Assessing suppression of gonadotropins using percentage of subjects with FSH and LH ≤ 1.0 IU/L.
Time frame: 2 months
Changes from baseline in sperm concentration.
Time frame: 4 - 6 months
Changes from baseline in LH level.
Time frame: 4 - 6 months
Changes from baseline in FSH level.
Time frame: 4 - 6 months
Changes from baseline in Testosterone level.
Time frame: 4 - 6 months
Changes from baseline in Estradiol level.
Time frame: 4 - 6 months
Changes from baseline in DHT level.
Time frame: 4 - 6 months
Changes from baseline in SHBG level.
Time frame: 4 - 6 months
Changes from baseline in DMA level.
Time frame: 4 - 6 months
Changes from baseline in DMAU level.
Time frame: 4 - 6 months
Changes from baseline in LNG level.
Time frame: 4 - 6 months
Incidence of treatment emergent adverse events (safety and tolerability) with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in sodium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in potassium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in bicarbonate with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in chloride with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in fasting glucose with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in blood urea nitrogen with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in creatinine with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in calcium with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in total bilirubin with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in alkaline phosphatase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in alanine aminotransferase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in aspartate transaminase with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in albumin with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in PSA with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone.
Time frame: 12 weeks
Changes from baseline in sexual function with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the psychosexual daily questionnaire.
Time frame: 12 weeks
Changes from baseline in prostate function with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the International Prostate Symptom Score.
Time frame: 12 weeks
Changes from baseline in mood with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone using the Patient Health Questionnaire-9.
Time frame: 12 weeks
Changes from baseline in blood pressure.
Time frame: 4 - 6 months
Changes from baseline in heart rate.
Time frame: 4 - 6 months
Changes from baseline in weight.
Time frame: 4 - 6 months
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 30 Oct 2025.
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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.
The record lists no contact. Use the official record to reach the sponsor.
2 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 Dimethandrolone-Undecanoate and Levonorgestrel 0.03 MG in people with Healthy and Men, run by Premier Research at 2 sites in United States.
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 30 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. 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?
Suppression of spermatogenesis as assessed by semen analyses using number of subjects with sperm concentration <3 million (M)/mL with daily oral dose of DMAU (3 different doses) alone or with LNG 30 mcg for 12 weeks versus placebo alone. (time frame: 12 weeks). 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 30 Oct 2025.