Phase 3 Spinal Muscular Atrophy Trial, Recruiting NCT07723248 Sponsor: ORIC Pharmaceuticals Condition: Spinal Muscular Atrophy
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Phase 3 Spinal Muscular Atrophy Trial, Recruiting

NCT07723248
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with prostate cancer (a specific type called adenocarcinoma, without small cell features), confirmed through a tissue or cell sample
  • People whose cancer has continued to grow or spread despite having their testosterone lowered through surgery or medication, and after receiving a treatment called abiraterone acetate (either for metastatic hormone-sensitive or early castration-resistant prostate cancer)
  • People whose cancer has spread to the bones (visible on a bone scan) or to soft tissues (visible on a CT or MRI scan)
  • People who are relatively well and able to carry out everyday activities, rated 0 or 1 on a standard medical scale called the ECOG performance scale
  • People whose organs (such as kidneys and liver) are functioning at an adequate level based on blood tests

Who may not be able to join:

  • People who have previously received certain prostate cancer treatments, including chemotherapy, radioligand therapy (such as lutetium-177 PSMA or radium-223), specific hormone-blocking drugs (apalutamide, darolutamide, or enzalutamide), PARP inhibitors used alone, or other systemic cancer treatments such as immunotherapy, antibody therapy, or gene/cell therapy — with two exceptions: (1) older-generation anti-hormone drugs (such as bicalutamide, flutamide, or nilutamide) are allowed if stopped before the first study dose, and (2) docetaxel chemotherapy is allowed if it was given for hormone-sensitive metastatic disease and the cancer did not progress during or within 3 months of finishing it
  • People who have received any other cancer treatment (drug or vaccine) within 28 days or 5 half-lives of the drug — whichever period is longer — before being enrolled (confirm with trial site)
  • People who have cancer that has spread to the brain, or who have active cancer involvement of the lining around the brain and spinal cord
  • People with significant heart or blood vessel disease (confirm with trial site for full details)
  • People with a serious medical condition, active infection (bacterial, fungal, or viral), or a psychiatric condition — including suicidal thoughts or behaviour within the past year — that in the treating doctor's judgment could increase the risk of participation or make the person unsuitable for the trial
  • People with active inflammatory bowel disease, ongoing chronic diarrhoea, or who have previously had stomach removal surgery or lap-band surgery

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
ORIC Pharmaceuticals
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 March 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Radiographic Progression Free Survival assessed by blinded independent central review (BICR) per RECIST v1.1 and Prostate Cancer Clinical Trials Working Group 3 (PCWG3)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov