Clinical Trials for Cancer Immunotherapy

Currently registered clinical trials for Cancer Immunotherapy from ClinicalTrials.gov. 29 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Cancer Immunotherapy from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 29
  • Active, not recruiting: 7
  • Completed: 5
  • Other: 9

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT01174121 — Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment332
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Cancer; Metastatic Pancreatic Cancer; Metastatic Ovarian Cancer; Metastatic Breast Carcinoma; Metastatic Endocrine Tumors/ Neuroendocrine Tumors
Interventions; ;

Background:

The NCI Surgery Branch has developed an experimental therapy that involves taking white blood cells from patients’ tumors, growing them in the laboratory in large numbers, and then giving the cells back to the patient. These cells are called Tumor Infiltrating Lymphocytes, or TIL and we have given this type of treatment to over 200 patients with melanoma. Researchers want to know i…

NCT01810913 — Testing Docetaxel-Cetuximab or the Addition of an Immunotherapy Drug, Atezolizumab, to the Usual Chemotherapy and Radiation Therapy in High-Risk Head and Neck Cancer

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorNational Cancer Institute (NCI)
Enrollment613
Study TypeINTERVENTIONAL
ConditionsOropharyngeal p16INK4a-Negative Squamous Cell Carcinoma; Stage III Hypopharyngeal Squamous Cell Carcinoma AJCC v7; Stage III Laryngeal Squamous Cell Carcinoma AJCC v6 and v7; Stage III Oral Cavity Squamous Cell Carcinoma AJCC v6 and v7; Stage III Oropharyngeal Squamous Cell Carcinoma AJCC v7
Interventions; ;

This phase II/III trial studies how well radiation therapy works when given together with cisplatin, docetaxel, cetuximab, and/or atezolizumab after surgery in treating patients with high-risk stage III-IV head and neck cancer the begins in the thin, flat cells (squamous cell). Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells a…

NCT03866382 — Testing the Effectiveness of Two Immunotherapy Drugs (Nivolumab and Ipilimumab) With One Anti-cancer Targeted Drug (Cabozantinib) for Rare Genitourinary Tumors

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment314
Study TypeINTERVENTIONAL
ConditionsBladder Adenocarcinoma; Bladder Clear Cell Adenocarcinoma; Bladder Mixed Adenocarcinoma; Bladder Neuroendocrine Carcinoma; Bladder Small Cell Neuroendocrine Carcinoma
Interventions; ;

This phase II trial studies how well cabozantinib works in combination with nivolumab and ipilimumab in treating patients with rare genitourinary (GU) tumors that has spread from where it first started (primary site) to other places in the body. Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such …

NCT05136196 — BiCaZO: A Study Combining Two Immunotherapies (Cabozantinib and Nivolumab) to Treat Patients With Advanced Melanoma or Squamous Cell Head and Neck Cancer, an immunoMATCH Pilot Study

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment150
Study TypeINTERVENTIONAL
ConditionsClinical Stage III Cutaneous Melanoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage IV Cutaneous Melanoma AJCC v8; Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Locally Recurrent Head and Neck Squamous Cell Carcinoma
Interventions; ;

This phase II trial studies the good and bad effects of the combination of drugs called cabozantinib and nivolumab in treating patients with melanoma or squamous cell head and neck cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed f…

NCT05442515 — CD19/CD22 Bicistronic Chimeric Antigen Receptor (CAR) T Cells in Children and Young Adults With Recurrent or Refractory B Cell Malignancies

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment130
Study TypeINTERVENTIONAL
ConditionsB-NHL; B-Non Hodgkin Lymphoma; Acute Lymphocytic Leukemia; Acute Lymphoblastic Leukemia; B-precursor ALL
Interventions; ;

Background:

Acute lymphoblastic leukemia (ALL) is the most common cancer in children. About 90% of children and young adults who are treated for ALL can now be cured. But if the disease comes back, the survival rate drops to less than 50%. Better treatments are needed for ALL relapses.

Objective:

To test chimeric antigen receptor (CAR) therapy. CARs are genetically modified cells created fro…

NCT06058377 — Adding an Immunotherapy Drug, MEDI4736 (Durvalumab), to the Usual Chemotherapy Treatment (Paclitaxel, Cyclophosphamide, and Doxorubicin) for Stage II-III Breast Cancer

StatusRecruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment3680
Study TypeINTERVENTIONAL
ConditionsAnatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; HER2-Negative Breast Carcinoma; Hormone Receptor-Positive Breast Carcinoma
Interventions; ;

This phase III trial compares the addition of an immunotherapy drug (durvalumab) to usual chemotherapy versus usual chemotherapy alone in treating patients with MammaPrint High 2 Risk (MP2) stage II-III hormone receptor positive, HER2 negative breast cancer. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body’s immune system attack the cancer, and may interfere with …

NCT05987241 — Testing the Role of DNA Released From Tumor Cells Into the Blood in Guiding the Use of Immunotherapy After Surgical Removal of the Bladder, Kidney, Ureter, and Urethra for Urothelial Cancer Treatment, MODERN Study

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorNational Cancer Institute (NCI)
Enrollment992
Study TypeINTERVENTIONAL
ConditionsMuscle Invasive Bladder Urothelial Carcinoma; Muscle Invasive Renal Pelvis Urothelial Carcinoma; Muscle Invasive Ureter Urothelial Carcinoma; Muscle Invasive Urethral Urothelial Carcinoma; Stage II Bladder Urothelial Carcinoma AJCC v6 and v7
Interventions; ;

This phase II/III trial examines whether patients who have undergone surgical removal of bladder, kidney, ureter or urethra, but require an additional treatment called immunotherapy to help prevent their urinary tract (urothelial) cancer from coming back, can be identified by a blood test. Many types of tumors tend to lose cells or release different types of cellular products including their DN…

NCT06140524 — A Proof-of-Concept Study to Learn Whether Linvoseltamab Can Eliminate Abnormal Plasma Cells That May Lead to Multiple Myeloma in Adult Patients With High-Risk Monoclonal Gammopathy of Undetermined Significance or Non-High-Risk Smoldering Multiple Myeloma

StatusRecruiting
PhasePhase 2
SponsorRegeneron Pharmaceuticals
Enrollment116
Study TypeINTERVENTIONAL
ConditionsMonoclonal Gammopathy of Undetermined Significance (MGUS); Smoldering Multiple Myeloma (SMM)
Interventions

This study is researching an investigational drug called linvoseltamab (“study drug”) in participants at moderate risk of developing multiple myeloma (about 3 to 10% average annual risk), a group that consists of patients with precancerous conditions called High-Risk Monoclonal Gammopathy of Undetermined Significance (HR-MGUS) and Non-High-Risk Smoldering Multiple Myeloma (NHR-SMM).

The primar…

NCT06545955 — A Trial to Evaluate Intravesical Nadofaragene Firadenovec Alone or in Combination With Chemotherapy or Immunotherapy in Participants With High-grade BCG Unresponsive Non-muscle Invasive Bladder Cancer

StatusRecruiting
PhasePhase 3
SponsorFerring Pharmaceuticals
Enrollment250
Study TypeINTERVENTIONAL
ConditionsNon-muscle Invasive Bladder Cancer With Carcinoma in Situ
Interventions; ;

The pivotal phase 3 trial (rAd-IFN-CS 003) evaluating the efficacy of nadofaragene firadenovec showed that 55 (53.4%) of 103 subjects with CIS ± high-grade Ta/T1 achieved a complete response (CR) at 3 months. In this trial, the safety and efficacy of intravesical instillation of nadofaragene firadenovec alone or in combination with chemotherapy or immunotherapy will be evaluated in participants…

NCT06788002 — LDRT and Chemoimmunotherapy in NPC With Liver Metastasis

StatusRecruiting
PhasePhase 2
SponsorHunan Cancer Hospital
Enrollment26
Study TypeINTERVENTIONAL
ConditionsNasopharyngeal Cancinoma (NPC)
Interventions

This study aims to evaluate the efficacy and toxicity of adding low-dose radiotherapy to chemoimmunotherapy as a first-line treatment for nasopharyngeal carcinoma patients with liver metastasis.

NCT06890598 — Study of Olomorasib (LY3537982) in Combination With Standard of Care in Participants With Resected or Unresectable KRAS G12C-mutant Non-Small Cell Lung Cancer

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment700
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Non-Small-Cell Lung
Interventions; ;

The main purpose of this study is to assess if olomorasib in combination with pembrolizumab is more effective than the pembrolizumab and placebo combination in part A in participants with resected KRAS G12C-mutant NSCLC and to assess if olomorasib in combination with durvalumab is more effective than the durvalumab and placebo combination in part B in participants with unresectable KRAS G12C-mu…

NCT06875310 — A Study of Adagrasib Plus Pembrolizumab Plus Chemotherapy vs. Placebo Plus Pembrolizumab Plus Chemotherapy in Participants With Previously Untreated Non-squamous Non-small Cell Lung Cancer With KRAS G12C Mutation (KRYSTAL-4)

StatusRecruiting
PhasePhase 3
SponsorMirati Therapeutics Inc.
Enrollment630
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Non-Small-Cell Lung
Interventions; ;

This is a trial to evaluate the efficacy, safety, and tolerability of adagrasib plus pembrolizumab plus platinum-doublet chemotherapy versus placebo plus pembrolizumab plus platinum-doublet chemotherapy in participants with previously untreated, locally advanced or metastatic NSCLC with KRAS G12C mutation

NCT06770582 — Testing the Addition of the Immunotherapy Drug, Pembrolizumab, to Radiation Therapy Compared to the Usual Chemotherapy Treatment During Radiation Therapy for Bladder Cancer, PARRC Trial

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment160
Study TypeINTERVENTIONAL
ConditionsNon-Muscle Invasive Bladder Urothelial Carcinoma; Recurrent Non-Muscle Invasive Bladder Urothelial Carcinoma; Stage I Bladder Cancer AJCC v8
Interventions; ;

This phase II trial compares the use of pembrolizumab and radiation therapy to chemotherapy with cisplatin, gemcitabine, 5-fluorouracil or mitomycin-C and radiation therapy for the treatment of non-muscle invasive bladder cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells…

NCT06317662 — Testing the Addition of the Anti-cancer Drug Venetoclax and/or the Anti-cancer Immunotherapy Blinatumomab to the Usual Chemotherapy Treatment for Infants With Newly Diagnosed KMT2A-rearranged or KMT2A-non-rearranged Leukemia

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment153
Study TypeINTERVENTIONAL
ConditionsAcute Leukemia of Ambiguous Lineage; B Acute Lymphoblastic Leukemia
Interventions; ;

This phase II trial tests the addition of venetoclax and/or blinatumomab to usual chemotherapy for treating infants with newly diagnosed acute lymphoblastic leukemia (ALL) with a KMT2A gene rearrangement (KMT2A-rearranged [R]) or without a KMT2A gene rearrangement (KMT2A-germline [G]). Venetoclax is in a class of medications called B-cell lymphoma-2 (Bcl-2) inhibitors. It may stop the growt…

NCT07106762 — Phase 2/3 Trial of Izalontamab Brengitecan vs Platinum-based Chemotherapy for Metastatic Urothelial Cancer With Disease Progression on or After Immunotherapy

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorBristol-Myers Squibb
Enrollment470
Study TypeINTERVENTIONAL
ConditionsUrothelial Cancer
Interventions; ;

A Phase 2/3 Trial of Izalontamab Brengitecan vs Platinum-based Chemotherapy for Metastatic Urothelial Cancer with Disease Progression on or After Immunotherapy

NCT06066138 — A Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment30
Study TypeINTERVENTIONAL
ConditionsLocally Advanced Alveolar Soft Part Sarcoma; Metastatic Alveolar Soft Part Sarcoma; Locally Advanced Non Small Cell Lung Cancer; Metastatic Non Small Cell Lung Cancer; Locally Advanced Small Cell Lung Cancer
Interventions

Background:

A type of drug called monoclonal antibody immune checkpoint inhibitors are often used in cancer treatment. These drugs help the body s immune system fight cancer by blocking proteins that cause cancer cells to grow. One of these drugs (atezolizumab) is approved to treat certain cancers. Researchers want to find out if lower doses of this drug might provide the same benefit with few…

NCT06931717 — A Clinical Study to Assess the Efficacy of Adjuvant Immunotherapy With Cemiplimab in Patients With Surgically Removed Non-small Cell Lung Cancer Who Have Not Received Prior Chemotherapy

StatusRecruiting
PhasePhase 3
SponsorETOP IBCSG Partners Foundation
Enrollment390
Study TypeINTERVENTIONAL
ConditionsNon-Small Cell Lung Cancer
Interventions

ARCH is a randomised, stratified, multicentre, phase III trial. Protocol treatment consists of cemiplimab, 350 mg i.v., every 3 weeks, for 4 cycles, followed by 700 mg i.v., every 6 weeks for 6 cycles or until relapse or unacceptable toxicities, whichever occurs first. The primary objective of the study is to determine the efficacy of adjuvant cemiplimab, as measured by disease-free survival, i…

NCT07198074 — Testing the Addition of an Antiangiogenic Drug (Bevacizumab) to Chemotherapy (Carboplatin and Paclitaxel) Combined With Immunotherapy (Pembrolizumab) for pMMR, TP53 Mutated Endometrial Cancer

StatusRecruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment255
Study TypeINTERVENTIONAL
ConditionsAdvanced Endometrial Carcinoma; Recurrent Endometrial Carcinoma
Interventions; ;

This phase III trial compares the effect of bevacizumab in combination with carboplatin, paclitaxel and pembrolizumab to the usual treatments of carboplatin and paclitaxel with or without pembrolizumab in treating patients with stage III, IVA or IVB mismatch repair protein proficient (pMMR) and TP53 mutated endometrial cancer that may have spread from where it first started to nearby tissue, ly…

NCT06900595 — Testing the Addition of an Anti-Cancer Drug, Cabozantinib to the Immunotherapy Drug Cemiplimab (REGN2810), in Adolescents and Adults With Advanced Adrenocortical Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment48
Study TypeINTERVENTIONAL
ConditionsLocally Advanced Adrenal Cortical Carcinoma; Metastatic Adrenal Cortical Carcinoma; Recurrent Adrenal Cortical Carcinoma; Stage III Adrenal Cortical Carcinoma AJCC v8; Stage IV Adrenal Cortical Carcinoma AJCC v8
Interventions; ;

This phase II trial compares the effect of giving cabozantinib with or without cemiplimab in patients with adrenocortical cancer that has spread to nearby tissue or lymph nodes (locally advanced), and that cannot be removed by surgery (unresectable) or that has come back after a period of improvement (recurrent) or that has spread from where it first started (primary site) to other places in th…

NCT07690540 — DETERMINANTS OF IMMUNOTHERAPY EFFICACY IN ENDOMETRIAL CANCER

StatusRecruiting
PhaseN/A
SponsorEuropean Institute of Oncology
Enrollment510
Study TypeINTERVENTIONAL
ConditionsEndometrial Cancer; Immune Checkpoint Inhibitors
Interventions

In recent years, the introduction of immune checkpoint inhibitors (ICI) in combination with chemotherapy has significantly changed the management of advanced and recurrent Endometrial Cancer (EC).

Despite these advances, responses to immunotherapy remain heterogeneous. Not all patients with mismatch repair-deficient (dMMR) tumors derive durable benefit, while a subset of mismatch repair-profic…

NCT07195734 — Testing the Addition of Chemotherapy or Chemo-Immunotherapy to the Usual Surgery for Advanced Head and Neck Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment180
Study TypeINTERVENTIONAL
ConditionsClinical Stage II HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8; Locally Recurrent Head and Neck Squamous Cell Carcinoma; Locally Recurrent Hypopharyngeal Squamous Cell Carcinoma; Locally Recurrent Laryngeal Squamous Cell Carcinoma
Interventions; ;

This phase II trial tests the addition of chemotherapy, with carboplatin and paclitaxel, or chemo-immunotherapy, with carboplatin, paclitaxel and cemiplimab to standard salvage surgery followed by post operative radiation therapy and cisplatin for high risk patients, for the treatment of patients with PD-L1 positive head and neck squamous cell carcinoma that has come back and spread to nearby t…

NCT07403136 — Becotatug Vedotin ± Anti-PD-1 in Pretreated Advanced ESCC

StatusRecruiting
PhasePhase 2
SponsorFudan University
Enrollment104
Study TypeINTERVENTIONAL
ConditionsEsophageal Squamous Cell Carcinoma
Interventions;

This study will test a new potential treatment for advanced esophageal squamous cell cancer (ESCC) for patients whose initial treatment has stopped working. Currently, the standard second-line treatment for this cancer is PD-1 inhibitors or chemotherapy alone, which is not very effective, allowing the cancer to grow again after just 1.6 to 3.4 months on average. Therefore, there is a strong nee…

NCT07242547 — Study of Tarlatamab as Maintenance Treatment After Chemo-radiotherapy for Limited Stage SCLC Patients

StatusRecruiting
PhasePhase 2
SponsorFundación GECP
Enrollment37
Study TypeINTERVENTIONAL
ConditionsLimited-stage Small-cell Lung Cancer; Carcinoma, Small Cell Lung; Respiratory Tract Neoplasms; Thoracic Neoplasms
Interventions

This is an open-label, phase II, exploratory and multi-centre clinical trial. 37 Limited stage SCLC patients not eligible for concurrent chemo-radiotherapy will be enroll.

Patients will be enrolled in the trial after receiving sequential chemo-radiotherapy, if there is no progression disease, patients will be treated with maintenance Tarlatamab.

Patients will receive maintenance with Tarlatam…

NCT07676461 — Oral, Fecal and Intratumoral Microbiome Atlas in Colombian Patients With Advanced Solid Tumors Receiving First-Line Immunotherapy

StatusRecruiting
PhaseN/A
SponsorCentro de Tratamiento e Investigación sobre Cáncer, Luis Carlos Sarmiento Angulo
Enrollment150
Study TypeOBSERVATIONAL
ConditionsGastric Cancer; Colorectal Cancer; Breast Cancer; Cervical Cancer; Head and Neck Cancer (H&N)
Interventions

This is a prospective observational cohort study conducted at Fundación CTIC in Bogotá, Colombia. It characterizes the oral, fecal and intratumoral microbiome of Colombian adults with advanced solid tumors (gastric, colorectal, breast, cervical and head-and-neck cancer) who receive first-line immunotherapy as standard of care, and compares them with healthy volunteers. Using multi-omics (HiFi m…

NCT07687875 — Oncolytic Virotherapy to Enhance PReoperative IMmunotherapy Efficacy in Patients With Proficient Mismatch Repair (pMMR) Rectal Cancer

StatusRecruiting
PhasePhase 1
SponsorHenry Smith
Enrollment20
Study TypeINTERVENTIONAL
ConditionsRectal Cancer Patients
Interventions

A Phase I clinical trial that will investigate the safety and tolerability of combining the modified vaccinia virus BT-001 with systemic pembrolizumab in patients with localised pMMR rectal cancer

NCT07280715 — Investigating Real-Time Immunotherapy Symptoms Study

StatusRecruiting
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment40
Study TypeINTERVENTIONAL
ConditionsCancer; Melanoma (Skin Cancer); Immunotherapy
Interventions;

The goal of this study is to evaluate the feasibility of using information from wearable devices and self-reported symptoms to remotely monitor patients during immunotherapy. The main questions it aims to answer are:

  • Is the digital remote patient monitoring tool feasible and acceptable to patients?
  • Do the alerts and guidance improve symptom management, quality of life, and engagement with …

NCT07689851 — Chemoradiotherapy and SHR-1701 in Patients With Unresectable Gastric Cancer

StatusRecruiting
PhasePhase 2
SponsorCancer Institute and Hospital, Chinese Academy of Medical Sciences
Enrollment60
Study TypeINTERVENTIONAL
ConditionsGastric Cancer (GC); Gastroesophageal Junction Adenocarcinoma
Interventions; ;

Gastric Cancer is one of the leading causes of cancer-related death worldwide, and patients with unresectable locally advanced or metastatic disease have a poor prognosis. This study aims to evaluate the safety and efficacy of radiotherapy combined with CAPOX and SHR-1701, a PD-L1/TGF-β bispecific antibody, in patients with unresectable locally advanced or metastatic gastric or gastroesophageal…

NCT06694454 — Neoadjuvant Inhaled Azacytidine With Platinum-Based Chemotherapy and Durvalumab (MEDI4736) - a Combined Epigenetic-Immunotherapy (AZA-AEGEAN) Regimen for Operable Early-Stage Non-Small Cell Lung Cancer (NSCLC)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsNon-small Cell Lung Cancer (NSCLC); Carcinoma, Non-Small Cell Lung; Non-Small Cell Lung Carcinoma; Non Small Cell Lung Cancer; Non Small Cell Lung Carcinoma
Interventions; ;

Background:

Lung cancer is the leading cause of cancer-related death worldwide. Non-small cell lung cancer (NSCLC) is the most common type of lung cancer. Surgery to remove the tumors is the standard treatment for people diagnosed with early stages of NSCLC. Despite complete removal of these tumors, many recur (happen again). An FDA-approved drug combination to treat early-stage NSCLC prior to…

NCT06904066 — Autologous T Cells Transduced With Retroviral Vectors Expressing TCRs for Participant-specific Neoantigens in Patients With Hematologic Malignancies

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment86
Study TypeINTERVENTIONAL
ConditionsMalignancy, Hematologic; Neoplasms, Hematologic; Neoplasms, Hematopoietic; Blood Cancer; Hematological Neoplasms
Interventions; ;

Background:

Blood cancers (such as leukemias) can be hard to treat, especially if they have mutations in the TP53 or RAS genes. These mutations can cause the cancer cells to create substances called neoepitopes. Researchers want to test a method of treating blood cancers by altering a person s T cells (a type of immune cell) to target neoepitopes.

Objective:

To test the use of neoepitope-spe…

Active, Not Recruiting

NCT02650986 — Gene-Modified T Cells With or Without Decitabine in Treating Patients With Advanced Malignancies Expressing NY-ESO-1

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorRoswell Park Cancer Institute
Enrollment15
Study TypeINTERVENTIONAL
ConditionsAdvanced Fallopian Tube Carcinoma; Advanced Malignant Solid Neoplasm; Advanced Melanoma; Advanced Ovarian Carcinoma; Advanced Primary Peritoneal Carcinoma
Interventions; ;

This phase I/IIa trial studies the side effects and best dose of gene-modified T cells when given with or without decitabine, and to see how well they work in treating patients with malignancies expressing cancer-testis antigens 1 (NY-ESO-1) gene that have spread to other places in the body (advanced). A T cell is a type of immune cell that can recognize and kill abnormal cells of the body. Pla…

StatusActive, not recruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment500
Study TypeOBSERVATIONAL
ConditionsMacrophage Activation Syndrome; Primary Hemophagocytic Lymphohistiocytosis

Immunotherapy is changing the landscape of cancer therapy. Particularly unique to immunotherapy is the toxicity profile, which differs from chemotherapy-based strategies and can be associated with inflammatory responses and/or autoimmune type reactions resulting from activation of the immune system. Referred to as immune related adverse events (irAEs), these adverse events may require systemic …

NCT03747120 — Neoadjuvant Her2-targeted Therapy and Immunotherapy With Pembrolizumab [IIT2018-04-MCARTHUR-NEOHP]

StatusActive, not recruiting
PhasePhase 2
SponsorUniversity of Texas Southwestern Medical Center
Enrollment138
Study TypeINTERVENTIONAL
ConditionsHER2-positive Breast Cancer; Breast Cancer
Interventions; ;

A phase 2 open-label, randomized, multi-center trial to evaluate the efficacy and safety of neoadjuvant trastuzumab, pertuzumab and weekly paclitaxel (THP) as compared to neoadjuvant trastuzumab, pertuzumab, pembrolizumab and weekly paclitaxel (THP-pembrolizumab), or neoadjuvant trastuzumab, pembrolizumab and weekly paclitaxel (TH-pembrolizumab ) in chemo naive patients with invasive human epid…

NCT03837899 — Durvalumab and Tremelimumab for Pediatric Malignancies

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorAstraZeneca
Enrollment50
Study TypeINTERVENTIONAL
ConditionsPediatric Cancer; Solid Tumor Pediatric; Hematological Malignancies
Interventions

The purpose of the study is to determine the recommended dose of durvalumab and tremelimumab (immunotherapy drugs) in pediatric patients with advanced solid and hematological cancers and expand in a second phase to test the efficacy of these drugs once this dose is determined.

NCT05507112 — TIME in Immunotherapy Combined With nCRT for Rectal Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorPeking Union Medical College Hospital
Enrollment100
Study TypeINTERVENTIONAL
ConditionsLocally Advanced Rectal Cancer
Interventions; ;

This is an open-label, prospective phase II clinical trial to evaluate the therapeutic and prognostic implications of tumor immune microenvironment in the neoadjuvant immunotherapy combined with chemoradiotherapy for patients with rectal cancer. A total of 100 patients will be enrolled in this trial. The primary endpoint is the complete response rate, defined as the proportion of patients who a…

NCT05502315 — Study of Cabozantinib and Nivolumab in Metastatic Castration Resistant Prostate Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorRana McKay, MD
Enrollment47
Study TypeINTERVENTIONAL
ConditionsCastration-resistant Prostate Cancer; Metastatic Cancer
Interventions;

This is a multicenter, single-arm, two-stage open-label phase 2 study of the combination of cabozantinib + nivolumab in subjects with advanced castration-resistant prostate cancer (CRPC).

NCT06165380 — Cardenilimab Combined With Chemotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma

StatusActive, not recruiting
PhasePhase 2
SponsorLi Zhang
Enrollment43
Study TypeINTERVENTIONAL
ConditionsEsophageal Squamous Cell Carcinoma; Neoadjuvant Therapies
Interventions

The goal of this trial is to test the efficacy and safety of cardenilimab combined with chemotherapy in the conversion therapy of locally advanced unresectable esophageal squamous cell carcinoma.

type of study: clinical trial

Not Yet Recruiting

NCT07686835 — Dietary Fiber to Induce Gut Microbiota-mediated Response to Immunotherapy in Melanoma.

StatusNot yet recruiting
PhasePhase 2
SponsorRadboud University Medical Center
Enrollment70
Study TypeINTERVENTIONAL
ConditionsMelanoma (Skin) Stage IV; Melanoma (Skin Cancer); Melanoma Metastatic; Melanoma Advanced; Melanoma
Interventions;

Previous research has shown that a higher fiber intake may have a beneficial effect on the intestinal health and improve the effectiveness of immunotherapy, but this is not certain. The objective of this double-blinded randomized clinical trial is to analyze, whether increased dietary fiber intake by patients with metastatic melanoma will increase the relative amount of Bifidobacterium, which i…

NCT07509034 — Autologous B7-H3 Chimeric Antigen Receptor T Cells in Previously Treated Extensive-Stage Small Cell Lung Cancer With Recurrent or Refractory Disease

StatusNot yet recruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment40
Study TypeINTERVENTIONAL
ConditionsExtensive-Stage Small Cell Lung Cancer; Extrapulmonary Neuroendocrine Carcinoma; Recurrent or Refractory; Solid Tumors
Interventions; ;

Background:

Small cell lung cancer (SCLC) is the deadliest form of lung cancer. Extrapulmonary neuroendocrine cancer (EPNEC) is a similar type of cancer that develops anywhere other than the lungs. EPNEC is also deadly. B7-H3 is a protein often found in SCLC and EPNEC tumor cells. Researchers can modify a person s own T cells, or immune cells, to target B7-H3. When these modified T cells are r…

NCT07574541 — Multitargeted Recombinant Ad5 PSA/MUC-1/Brachyury-Based Immunotherapy (TriAdeno) Vaccine With IL-15 Superagonist N-803 in Participants With Clinically Localized Prostate Cancer Undergoing Active Surveillance

StatusNot yet recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment52
Study TypeINTERVENTIONAL
ConditionsAdenocarcinoma; Prostate Cancer; Neoplasms; Carcinoma; Neoplasms, Glandular and Epithelial
Interventions;

Background:

Prostate cancer is the second most common cause of cancer-related death among men in the United States. Early-stage, low-grade prostate cancer is managed with active monitoring. However, 35% of men with this cancer will need treatment within 5 years because of tumor growth. Researchers want to know if a new vaccine that targets 3 anti-cancer proteins (TriAdeno) plus a drug (N-803) …

NCT07572136 — Anti-CRLF2-R/TSLPR Chimeric Antigen Receptor T Cells (TSLPR-CART) in Participants With Recurrent or Refractory CRLF2-R/TSLPR-Overexpressing B-Cell Acute Lymphoblastic Leukemia (B-ALL)

StatusNot yet recruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment57
Study TypeINTERVENTIONAL
ConditionsB-All; Acute Lymphoblastic Leukemia
Interventions; ;

Background:

B-cell acute lymphoblastic leukemia (B-ALL) is a type of blood cancer. Some people with B-ALL have a gene mutation that makes the disease hard to treat. The mutation causes cancer cells to make too much of a protein called thymic stromal lymphopoietin receptor (TSLPR). Chimeric antigen receptor (CAR) T cell therapy is a treatment that takes immune cells (T cells) from a person s bo…

NCT07686640 — Short-Course Radiotherapy Followed by CAPOX With or Without Iparomlimab and Tuvonralimab in pMMR/MSS Locally Advanced Rectal Cancer

StatusNot yet recruiting
PhasePhase 3
SponsorShandong Cancer Hospital and Institute
Enrollment180
Study TypeINTERVENTIONAL
ConditionsLocal Advanced Rectal Cancer; Radiotherapy; Immunotherapy
Interventions; ;

This multicenter, randomized, controlled, phase III trial evaluates whether adding iparomlimab and tuvonralimab injection to CAPOX consolidation chemotherapy after short-course radiotherapy improves tumor response in patients with treatment-naive, proficient mismatch repair/microsatellite-stable (pMMR/MSS) locally advanced rectal adenocarcinoma. Eligible patients will be randomly assigned in a …

NCT07545954 — DSP-0390 in Combination With Atezolizumab for Small Cell Lung Cancer

StatusNot yet recruiting
PhasePhase 1
SponsorWashington University School of Medicine
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSmall-cell Lung Cancer; Small Cell Lung Cancer Extensive Stage
Interventions;

This is a single center pilot, phase Ib study with a safety lead-in evaluating the safety and preliminary efficacy of the EBP inhibitor DSP-0390 in combination with atezolizumab in patients with extensive stage small cell lung cancer (ES-SCLC) whose disease has not progressed after initial induction therapy with platinum-based chemotherapy and anti-PD-L1 immunotherapy (atezolizumab or durvaluma…

NCT07690683 — Patients With Hepatocellular Carcinoma (HCC)

StatusNot yet recruiting
PhaseN/A
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment52
Study TypeINTERVENTIONAL
ConditionsHepatocellular Carcinoma; Hepatocellular Cancer; Liver Diseases; Liver Cancer
Interventions;

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide and is frequently diagnosed at an advanced stage, resulting in limited therapeutic options. Despite the advances in immunotherapy, a substantial proportion of patients fail to respond adequately due to mechanisms of immune resistance. The gut microbiota plays a crucial role in modulating the respon…

Completed Trials

NCT02710253 — Salvage Radiation Therapy in Treating Patients With Metastatic Cancer That Has Progressed After Systemic Immunotherapy

StatusCompleted
PhasePhase 2
SponsorM.D. Anderson Cancer Center
Enrollment214
Study TypeINTERVENTIONAL
ConditionsHematopoietic and Lymphoid Cell Neoplasm; Metastatic Malignant Solid Neoplasm
Interventions; ;

This phase II trial studies the side effects and best dose of radiation therapy and to see how well it works in treating patients with cancer that has spread to other places in the body (metastatic) or has increased in size after being treated with immunotherapy. Giving radiation therapy may help to control the cancer after the disease has gotten worse after receiving immunotherapy in patients …

NCT03603808 — VGX-3100 and Electroporation in Treating Patients With HIV-Positive High-Grade Anal Lesions

StatusCompleted
PhasePhase 2
SponsorAIDS Malignancy Consortium
Enrollment44
Study TypeINTERVENTIONAL
ConditionsAnal Intraepithelial Neoplasia; High Grade Squamous Intraepithelial Neoplasia; HIV Positivity; Human Papillomavirus-16 Positive; Human Papillomavirus-18 Positive
Interventions; ;

This phase II trial studies the use of human papillomavirus (HPV) deoxyribonucleic acid (DNA) plasmids therapeutic vaccine VGX-3100 (VGX-3100) and electroporation in treating patients with human immunodeficiency virus (HIV)-positive high-grade anal lesions. Vaccines made from DNA may help the body build an effective immune response to kill tumor cells. Electroporation helps pores in your body’s…

NCT04656873 — Immuno-Oncology Database and Bioregistry

StatusCompleted
PhaseN/A
SponsorUNC Lineberger Comprehensive Cancer Center
Enrollment32
Study TypeOBSERVATIONAL
ConditionsMalignancy; Immune System Diseases; Autoimmune Diseases
Interventions; ;

Immunotherapy, especially immune checkpoint inhibitors (ICIs), are effective in treating many different types of cancers. ICIs fight cancer by driving the immune system into an “activated state” that makes it harder for tumor cells to hide and easier for the immune system to destroy them. In doing this, oncologists risk “over activation” where immune cells can cause side effects that could affe…

NCT04926948 — Stereotactic Body Radiation Therapy With Immunotherapy for the Treatment of Mesothelioma

StatusCompleted
PhasePhase 1
SponsorMayo Clinic
Enrollment20
Study TypeINTERVENTIONAL
ConditionsPleural Mesothelial Neoplasm
Interventions; ;

This phase I trial studies the effect of stereotactic body radiation therapy and immunotherapy in treating patients with mesothelioma. Stereotactic body radiation therapy uses special equipment to position a patient and deliver radiation to tumors with high precision. This method may kill tumor cells with fewer doses over a shorter period and cause less damage to normal tissue. Giving stereotac…

NCT06636591 — Pilot Study of Neoadjuvant Chemotherapy Combined With Immunotherapy and Multimodal Thermal Therapy for HER2-negative Breast Cancer

StatusCompleted
PhaseN/A
SponsorFudan University
Enrollment14
Study TypeINTERVENTIONAL
ConditionsBreast Cancer Female; HER2-negative Breast Cancer
Interventions;

In this study, breast cancer (BC) patients eligible for inclusion will be divided into two groups according to molecular typing and subtyping, which combined immunotherapy and multimodal thermal therapy with conventional neoadjuvant chemotherapy, to explore methods of immune induction for BC, enhance the efficacy of immunotherapy, and accumulate data for subsequent stages of clinical study.

Other (Suspended)

NCT07388563 — Azacitidine and Abatacept in Relapsed or Refractory T-Cell Lymphoma

StatusSuspended
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment20
Study TypeINTERVENTIONAL
ConditionsLymphoma, T Cell, Peripheral; T-cell Lymphoma; Angioimmunoblastic T-cell Lymphoma; Anaplastic Large Cell Lymphoma; Monomorphic Epitheliotropic Intestinal T-cell Lymphoma
Interventions;

Background:

T-cell lymphoma is a blood cancer that affects immune system cells. People tend to survive less than 1 year if this disease does not respond to treatment (is refractory) or comes back after treatment (relapses). Azacitidine and abatacept are 2 drugs that are used to treat other diseases. Researchers want to know if these drugs, used together, can help people with T-cell lymphoma.

NCT05642195 — Evaluation of a Cancer Lysate Vaccine and Montanide (Registered Trademark) ISA-51 VG With or Without the IL-15 Super-Agonist N-803 as Adjuvant Therapy for PD-L1 Negative Non-Small Cell Lung Cancer

StatusSuspended
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment30
Study TypeINTERVENTIONAL
ConditionsNon-Small Cell Lung Cancer; Non-Small Cell Lung Carcinoma; Carcinoma, Non-Small-Cell Lung; Carcinomas
Interventions; ;

Background:

Surgery is the primary treatment for non-small cell lung cancer (NSCLC) that is diagnosed in its earlier stages. But the tumors often return. Radiation and chemotherapy can improve survival in some people who have had surgery for NSCLC, but these treatments also cause serious side effects. A new approach, called immunotherapy, may be a better way to stop NSCLC tumors from coming ba…