NCT06111781 The SUGAR Study; SBRT and Relugolix) for Prostate Cancer
| NCT ID | NCT06111781 |
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Yale University |
| Condition | Prostate Cancer |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2024-04-15 |
| Primary Completion | 2028-02 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.
This trial targets 60 participants in total. It began in 2024-04-15 with a primary completion date of 2028-02.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The goal of this clinical trial is to measure the toxicity and effectiveness of the following treatments for cFIR/cgUIR prostate cancer patients. Stereotactic body radiotherapy (SBRT) alone or Stereotactic body radiotherapy (SBRT) combined with Ultrashort GNRH Antagonist called Relugolix (an oral drug). Treatments will be randomly assigned to study patients. The main questions it aims to answer are the following: 1. Whether the proportion of men who undergo SUGAR have superior rate of attaining PSA nadir of \<= 0.2 compared to SBRT alone, and 2. Whether SUGAR is superior to historical rates of minimal clinically important decline (MCID) in sexual and hormonal function at 6 months for patients undergoing 6 months of androgen deprivation therapy (ADT) Men aged 18+ with cFIR/cgUIR will be enrolled. Specifically, patients must meet one of the following 2 criteria: 1) Gleason score must be Gleason 3+4 with a PSA \< 20 ng/mL, or 2) Gleason 6 (3+3) and PSA \> 10 ng/mL and \< 20 ng mL.
Eligibility Criteria
Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Has histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate 4. Born assigned to Male gender, age 18 and above. Female identifying transgender or gender fluid are allowed on study provided they have not undergone testosterone suppressing therapy and were born with a prostate. 5. Has a serum testosterone at the Screening visit of \>100 ng/dL 6. Has a serum PSA concentration at the Screening visit of \> 0.2 ng/mL 7. Able to swallow pills and take medication orally (no documented inability to eat solids and swallow pills) and be willing to adhere to the daily regimen of medication (if assigned to the experimental arm). 8. For patients of reproductive potential: use of condoms or other methods (including abstinence) to ensure effective contraception with partner during radiotherapy and through 4 months after the last dose of the study drug or radiotherapy 9. Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration 10. Clinical favorable intermediate risk prostate cancer: Gleason score must be Gleason 3+4 with a PSA \< 20 ng/mL, or Gleason 6 (3+3) and PSA \> 10 ng/mL and \< 20 ng mL. 11. Decipher GC score of 0.6 or higher or higher indicating high genomic risk for most recent biopsy 12. Documented prostate volume (by MRI or ultrasound within 120 days or physician attestation within 120 days) \<= 80 cc Exclusion Criteria: 1. Current use of medications that cause QT prolongation 2. Known allergic reactions to relugolix 3. Treatment with another investigational drug or other intervention for prostate cancer within 30 days of enrollment 4. Ulcerative colitis or other inflammatory bowel disease history 5. Connective tissue disease such as lupus, scleroderma, or dermatomyositis 6. GNRH antagonist therapy or SBRT to the prostate are medically contraindicated or not tolerated 7. History of long QT syndrome documented in the medical record 8. The following ECG abnormalities are excluded: 1. Q-wave infarction unless identified 6 or more months before the Screening Visit 2. QT interval corrected for heart rate (QTc) \> 470 msec. If the QTc is prolonged in a patient with a pacemaker, the patient may be enrolled in the study upon discussion with the study PI 3. Congenital long QT syndromeQ 9. History of surgical castration 10. Prior treatment for prostate cancer with surgery or prostate directed radiotherapy
Contact & Investigator
James Yu
PRINCIPAL INVESTIGATOR
Yale University
Frequently Asked Questions
Who can join the NCT06111781 clinical trial?
This trial is open to male participants only, aged 18 Years or older, studying Prostate Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
What phase is the NCT06111781 trial and what does that mean for participants?
Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.
Is NCT06111781 currently recruiting?
Yes, NCT06111781 is actively recruiting participants. Contact the research team at camalene.chrysostoum@yale.edu for enrollment information.
Where is the NCT06111781 trial being conducted?
This trial is being conducted at New Haven, United States, New York, United States, Seattle, United States.
Who is sponsoring the NCT06111781 clinical trial?
NCT06111781 is sponsored by Yale University. The principal investigator is James Yu at Yale University. The trial plans to enroll 60 participants.
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