Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Study of NMS-03305293 in Adult Patients With Relapsed Ovarian Cancer

This is a multicenter, open-label Phase Ia/b study on the safety and efficacy of the combination of NMS-03305293 and topotecan in patients with recurrent ovarian cancer, with dose-limiting toxicity (DLT) escalation. The aim of this study is to determine the safety and tolerability, as well as to evaluate the anti-tumor efficacy and pharmacokinetics of NMS-03305293 in combination with topotecan.

Participants needed: 24
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: Nerviano Medical SciencesUpdated: May 28, 2026Locations: 5
Eligibility criteria

Histologically confirmed diagnosis of high-grade serous epithelial ovarian, fall... [+5]

Current enrollment in another interventional clinical trial. [+23]

Status: Recruiting

Study of NMS-03305293 in Adult Patient With Relapsed Small Cell Lung Cancer

This is an open-label study of NMS-03305293 with Temozolomide (TMZ) in patients with Small Cell Lung Cancer (SCLC). The aim of this study is to determine the safety and tolerability, as well as to evaluate the anti-tumor efficacy and pharmacokinetics of NMS-03305293 in combination with TMZ.

Participants needed: 10
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Nerviano Medical SciencesUpdated: Nov 12, 2025Locations: 2
Eligibility criteria

Histologically confirmed extensive-stage Small Cell Lung Cancer (SCLC); must hav... [+6]

Current enrollment in another interventional clinical trial. [+18]

Status: Recruiting

Study of NMS-03597812 in Adult Patients With Relapsed/Refractory Acute Myeloid Leukemia

The aim of PERKA-812-003 study is to investigate the safety, pharmacokinetics and preliminary anti-tumor activity of treatment with NMS-03597812 as single agent in Relapsed/Refractory Acute Myeloid Leukemia (R/R AML) patients who have exhausted standard treatment, including a subset of patients with TP53 mutations. It is anticipated that combination with venetoclax will be further evaluated following a future protocol amendment, once the Recommended Range Dose (RDR) as single agent has been defined.

Participants needed: 124
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Nerviano Medical SciencesUpdated: Oct 31, 2025Locations: 7
Eligibility criteria

single agent dose escalation of NMS-03597812: R/R AML patients who have exhauste... [+11]

Current enrollment in another interventional clinical study unless only particip... [+17]