Fanconi anemia complementation group N
Fanconi anemia complementation group N
Explore linked clinical trials. Standard reference: MONDO:00125652 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Carboplatin or Olaparib for BRcA Deficient Prostate Cancer | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fanconi anemia complementation group D1, Fanconi anemia complementation group N, Genital Diseases, Male Urogenital Diseases, Neoplasms by Site, Urogenital Diseases, Urogenital Neoplasms, central nervous system malformation, hereditary disease, hereditary sensory and autonomic neuropathy, inherited neurodegenerative disorder, male reproductive organ cancer, male reproductive system disorder, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, prostate cancer, prostate disorder | Recruiting | Phase 2 | 2026-09-17 | NCT04038502 | |
| Study to Assess Safety, Tolerability and Activity of DSB2455 in Participants With Advanced Malignancies | Fanconi anemia complementation group D1, Fanconi anemia complementation group N, microphthalmia, syndromic 9 | Recruiting | Phase 1 | 2026-09-02 | NCT06458712 |