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

CB-103 With Either Lenvatinib or Abemaciclib in Patients With NOTCH ACC

The goal of this study is to treat patients with NOTCH active advanced adenoid cystic carcinoma (ACC) tumors with a combination or two different oral medications to slow tumor growth and improve survival outcomes. The names of the study drugs involved in this study are: * CB-103 (an oral NOTCH pathway inhibitor) * Abemaciclib (CDK4/6 inhibitor) * Lenvatinib (a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor (TKI))

Participants needed: 32
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Glenn J. HannaUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Participants must have histologically confirmed adenoid cystic carcinoma (ACC) w... [+13]

Participant has untreated or clinically symptomatic CNS metastases and/or carcin... [+8]

Status: Recruiting

PD-L1 t-haNK, NAI IL-15sa and Cetuximab for Recurrent, Metastatic HNSCC

The purpose of this research study is to test the safety and efficacy of the combination of PD-L1 t-haNK (modified immune cells), NAI (a manufactured protein that stimulates the immune system), and cetuximab (a targeted antibody) in treating advanced head and neck cancer. The names of the therapies involved in this study are: * PD-L1 t-haNK cell therapy (a NK cell therapy infusion) * NAI (a type of recombinant human superagonist) * Cetuximab (a type of antibody)

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Glenn J. HannaUpdated: Jun 11, 2026Locations: 2
Eligibility criteria

Participants must have an existing histologically confirmed diagnosis of head an... [+15]

Have been previously treated with 3 or more lines of systemic therapy for R/M HN... [+8]

Status: Recruiting

Phase II Study of RP2 as Immunoprevention in High-Risk Oral Precancerous Disease

The goal of this study is to understand the safety, tolerability, and potential efficacy of an injected immune therapy called RP2 to treat oral precancer conditions and prevent progression to an oral cancer. The name of the study drug involved in this study is: -RP2 (a genetically modified live Herpes Simplex V-1 strain)

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Glenn J. HannaUpdated: Apr 23, 2026Locations: 2
Eligibility criteria

Proliferative leukoplakia (PL) [+15]

Prior treatment with an oncolytic virus therapy. [+10]

Status: Recruiting

A Phase 2 Trial of Ivonescimab for Patients With Advanced, Metastatic Salivary Gland Cancers

The goal of this study is to evaluate the efficacy and safety of Ivonescimab in participants with advanced, metastatic salivary gland cancers. The name of the study drug involved in this study is: -Ivonescimab (a type of antibody)

Participants needed: 35
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Glenn J. HannaUpdated: Jul 29, 2025Locations: 2
Eligibility criteria

Participants must have histologically confirmed salivary gland carcinoma (any hi... [+18]

Participant has known active central nervous system (CNS) metastases and/or carc... [+18]

Status: Recruiting

Toripalimab With Chemotherapy for Sinus Cancer

The aim of this research study is to evaluate the effectiveness and safety of a combination of immunotherapy, using a drug called toripalimab, with chemotherapy drugs, Carboplatin and Docetaxel, as a possible treatment before surgery for sinonasal cancers. The names of the study drugs used in this research study are: * Toripalimab (a type of monoclonal antibody) * Carboplatin (a type of antineoplastic agent) * Docetaxel (a type of antineoplastic agent) * Cisplatin (a type of antineoplastic agent)

Participants needed: 20
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Glenn J. HannaUpdated: Jun 26, 2025Locations: 2
Eligibility criteria

Participants must have histologically or cytologically confirmed locoregionally... [+14]

Participants with nasal cavity or paranasal sinus malignancies demonstrating his... [+12]