Clinical trials

4

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

Condition / disease
Location
Status: Recruiting

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of INV-8989 in Patients With Advanced Solid Tumors Harboring KRAS G12D Mutations

This is a Phase 1 and Phase 2 study to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of INV-8989 in patients with advanced solid tumors harboring KRAS G12D mutations.

Participants needed: 178
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen Ionova Life Sciences Co., Ltd.Updated: Jun 10, 2026Locations: 1
Eligibility criteria

Written informed consent obtained. [+9]

Have protocol-defined toxicities within 28 days before the start of study treatm... [+17]

Status: Recruiting

A Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of INV-9956 in Adult Patients With Advanced Metastatic Castration Resistant Prostate Cancer

This is a Phase 1 and Phase 2 study to evaluate the safety and antitumor activity of INV-9956 in adult patients with advanced metastatic Castration Resistant Prostate Cancer.

Participants needed: 84
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Shenzhen Ionova Life Sciences Co., Ltd.Updated: Jun 4, 2026Locations: 22
Eligibility criteria

Written informed consent obtained. [+11]

Have a medical condition such as Crohn's disease or have undergone significant s... [+8]

Status: Recruiting

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of INV-6452 in Adult Patients With Hormone Receptor Positive, Human Epidermal Growth Factor Receptor 2 Negative (HR+/HER2-) Advanced/Metastatic Breast Cancer or Locally Advanced/Metastatic Solid Tumor

This is a Phase 1 and Phase 2 study to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of INV-6452 in adult patients with Hormone Receptor Positive, Human Epidermal Growth Factor Receptor 2 Negative (HR+/HER2-) advanced/metastatic breast cancer or locally advanced/metastatic solid tumor.

Participants needed: 201
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen Ionova Life Sciences Co., Ltd.Updated: May 29, 2026Locations: 1
Eligibility criteria

Written informed consent obtained. [+8]

Have a second primary malignancy. [+19]

Status: Recruiting

An Open-Label Study of INV-1120 as a Single Agent and in Combination With Pembrolizumab in Adult Patients With Advanced Solid Tumors

Phase 1, open-label dose-escalation study to determine the MTD of INV-1120 and RP2D, and to assess the DLT of INV-1120 as a single agent or in the combination with pembrolizumab. The safety, tolerability, and PK of INV-1120 as a single agent or in the combination with pembrolizumab will be assessed in adult patients with advanced solid tumors.

Participants needed: 78
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen Ionova Life Sciences Co., Ltd.Updated: Mar 18, 2026Locations: 3
Eligibility criteria

Written informed consent, according to local guidelines, signed and dated by the... [+10]

History (≤5 years) or current evidence of cancer that is histologically distinct... [+30]