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There are 746 active trials for advanced/metastatic other solid tumor. Click on a trial to see more information. Note that this list also includes some trials that are only for specific cancer types like lung cancer. To see trials customized to a patient, please select a patient above.
746 trials meet filter criteria.
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HealthScout AI summary: This trial enrolls adults with advanced, FAP-positive solid tumors who have progressed on or lack standard therapy, using [203Pb]Pb-PSV359 SPECT imaging to confirm FAP expression and [212Pb]Pb-PSV359, a FAP-targeted alpha-emitting peptide-radiopharmaceutical, for systemic therapy.
ClinicalTrials.gov ID: NCT06710756
HealthScout AI summary: This trial is enrolling adults with advanced or metastatic colorectal, ovarian, fallopian tube, primary peritoneal, endometrial, cervical, or non-small cell lung cancers who have progressed on standard therapies, to receive PHN-010, an investigational antibody-drug conjugate targeting a tumor-associated antigen (target undisclosed) with a cytotoxic payload. Eligible patients must have measurable disease, ECOG 0-1, prior systemic therapy, and no remaining standard treatment options.
ClinicalTrials.gov ID: NCT06457997
HealthScout AI summary: This trial enrolls adults with advanced solid tumors that are mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H), including those with previously treated colorectal or endometrial cancer, to receive the investigational oral Werner DNA helicase (WRN) inhibitor GSK4418959—alone or combined with a PD-1 inhibitor—to target DNA repair vulnerabilities in these tumors. Patients must have exhausted standard treatment options and have good performance status.
ClinicalTrials.gov ID: NCT06710847
HealthScout AI summary: This trial evaluates the safety and maximum tolerated dose of INBRX-106, a hexavalent OX40 agonist antibody, both alone and in combination with pembrolizumab, in adult patients with locally advanced or metastatic solid tumors, including NSCLC, melanoma, and head and neck squamous cell carcinoma, who have progressed on standard therapies.
ClinicalTrials.gov ID: NCT04198766
HealthScout AI summary: This trial targets adult patients with advanced solid tumors, including NSCLC, melanoma, liposarcoma, leiomyosarcoma, and SCCHN, who have exhausted standard treatments. It evaluates OR2805, a monoclonal antibody targeting CD163 to modulate tumor-associated macrophages, administered alone or with cemiplimab or docetaxel.
ClinicalTrials.gov ID: NCT05094804
HealthScout AI summary: This trial assesses BT8009, a Bicycle Toxin Conjugate targeting Nectin-4, both as monotherapy and combined with pembrolizumab, in patients with advanced Nectin-4 expressing solid tumors such as urothelial carcinoma, breast, NSCLC, and ovarian cancers, who have progressed after prior treatment or lack standard therapy options. The study evaluates safety, pharmacokinetics, and preliminary efficacy, with previously reported promising response rates in treated urothelial cancer patients.
ClinicalTrials.gov ID: NCT04561362
HealthScout AI summary: The trial investigates the use of AG01, an anti-progranulin/GP88 monoclonal antibody, in patients with relapsed or refractory advanced solid tumors, including triple negative breast cancer, hormone-resistant breast cancer, non-small cell lung cancer, and mesothelioma, who have no remaining effective treatment options. AG01 is administered biweekly to evaluate its safety, tolerability, and preliminary anti-tumor activity.
ClinicalTrials.gov ID: NCT05627960
HealthScout AI summary: This trial is focused on patients with metastatic or locally advanced solid tumors, specifically colorectal cancer and non-small cell lung cancer, investigating the safety and efficacy of EU101, an agonistic monoclonal antibody targeting the 4-1BB receptor to enhance immune response.
ClinicalTrials.gov ID: NCT04903873
HealthScout AI summary: This trial involves adult patients with advanced or metastatic solid tumors such as melanoma and non-small cell lung cancer who have relapsed after standard treatments, testing the investigational agent ST-067 alone or with pembrolizumab and obinutuzumab to enhance immune response against tumor cells.
ClinicalTrials.gov ID: NCT04787042
HealthScout AI summary: This trial enrolls adults with advanced solid tumors harboring RET gene abnormalities, including both NSCLC and other solid tumors, regardless of prior RET inhibitor exposure. Patients receive TAS0953/HM06 (vepafestinib), an oral selective RET tyrosine kinase inhibitor active against resistance mutations and designed for enhanced CNS penetration.
ClinicalTrials.gov ID: NCT04683250
