Sign in
Taking people in United StatesPhase 2

Testosterone Replacement in Male Cancer Survivors With Fatigue and Low Testosterone

Key facts

Who runs it
Seattle Institute for Biomedical and Clinical Research
Where
Boston and Seattle, United StatesSee the 2 sites
Trial code
Status
Recruiting
Phase
Phase 2
People taking part
240 people, planned
Started
22 Mar 2021
Expected to end
30 Jan 2027
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • Testosterone Undecanoate 750 MG/3 ML Intramuscular Solution [AVEED]
  • placebo
Record updated
22 June 2026

Who can take part

Age
18 years to 54 years
Sex
Men only
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 21 criteriaShow less

Who can take part

  • Cancer survivors who have received chemotherapy and/or radiation therapy for their cancer and are now in remission for at least one year
  • Non-hormone-dependent cancer, including most solid tumors, lymphomas and leukemias
  • Age: 18-54 years
  • Serum testosterone, measured by mass spectrometry (gold standard method), of <348 ng/dl and/or free testosterone <70 pg/ml. The lower limits of the normal range for total testosterone in healthy young men (age 19-40 years), is 348 ng/dL and the lower limits of free testosterone is <70 pg/ml in the Framingham Heart Study sample97. Therefore, young symptomatic men with total testosterone <348 ng/dl could be considered testosterone deficient. As sex hormone binding globulin levels may be elevated in some men with cancer (resulting in elevation in total testosterone level), some of these symptomatic men may still be hypogonadal despite having total testosterone above this cut-off limit. However; their free testosterone levels may still be below the lower limit of normal. Thus, we will also include men with free testosterone <70 pg/mL
  • Self-reported fatigue. We have selected these symptoms because they are commonly reported in male cancer survivors. Fatigue will be defined as a score on Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F) subscale of <40, which best divides cancer patients from the general population with 84% accuracy, and was used as the cut-off for the NIA-funded 50-million-dollar testosterone trial (The T-Trial)
  • Ability and willingness to provide informed consent

Who cannot take part

  • Myocardial infarction, acute coronary syndrome, revascularization surgery, or stroke within 3 months; o Previous stroke with residual cognitive or functional deficits; Mini-Mental State Examination score <24
  • Untreated unipolar depression (treated depression with medications or counseling will be allowed
  • Men with hormone-dependent cancers (breast, prostate or adenocarcinoma of unknown origin)
  • Men with brain cancer (potential cognitive impairment)
  • Men with 1st order relatives with a history of prostate cancer
  • Uncontrolled congestive heart failure
  • Bipolar disorder or schizophrenia
  • Serum creatinine >2.5 mg/dL; ALT 3x upper limit of normal
  • Poorly controlled diabetes as defined by hemoglobin A1c >8.5%; Body mass index (BMI) >45 kg/m2
  • Use of anabolic agents (testosterone, dehydroepiandrosterone, growth hormone) within the past 6 months
  • Appetite stimulating agents e.g. megestrol acetate within the past 6 months
  • Systemic glucocorticoids e.g. prednisone 20 mg daily or equivalent doses of other glucocorticoids for more than two weeks in the past 6 months
  • Baseline hematocrit >48%
  • PSA >4 ng/ml in Caucasians; >3 ng/ml in African-Americans
  • Severe untreated sleep apnea

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 54 years old?

Where in United States

  • Brigham and Women's HospitalBoston, United StatesContact: Milena Braga, MDTaking people
  • Veterans Affairs Puget Sound Health Care SystemSeattle, United StatesContact: Gary Miranda, LPNTaking people

About the trial

What the trial wants to find out

The overall goal of this study is to evaluate the effect of a testosterone drug called Depo-Testosterone (or 'testosterone cypionate'), an FDA-approved drug for improving fatigue, sexual function, quality of life, body composition, muscle strength, and physical activity in young cancer survivors who report fatigue and have low testosterone. Main hypothesis is that Testosterone administration in young male cancer survivors who are in remission for at least 1 year, report cancer-related fatigue and have symptomatic testosterone deficiency will be associated with greater improvements in fatigue scores compared with placebo.

The 2 groups in the trial

  • TestosteroneTreatment being tested

    Testosterone undecanoate injection 750 MG/3 ML

    Treatment: Testosterone Undecanoate 750 MG/3 ML Intramuscular Solution [AVEED]

  • PlaceboPlacebo, for comparison

    clinical grade saline 0.9% sodium chloride injection

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Improving Patient-Important Outcomes With Testosterone Replacement in Hypogonadal Men With a Prior History of Cancer
Fit questions
Built from NCT04049331, who can take part
Record updated
22 June 2026