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 Kidney Cancer from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 29
- Active, not recruiting: 10
- Completed: 5
- Other: 6
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00026884 — Collection of Serum and Tissue Samples From Patients With Biopsy-Proved or Suspected Malignant Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 5950 |
| Study Type | OBSERVATIONAL |
| Conditions | Malignant Neoplasms; Hereditary Neoplastic Syndromes; Kidney Cancer; Renal Cancer; Bladder Cancer |
Selected individuals suspected of having or with prior biopsy proof of malignant disease will be seen in the Urologic Oncology Branch, NCI. Blood samples may be collected at the time of the initial visit and at periodic intervals during the course of the disease. These samples will be stored in the tissue bank of the Urologic Oncology Branch. Aliquots of malignant and normal tissue will be coll…
NCT00050752 — Hereditary Leiomyomatosis Renal Cell Cancer - Study of the Genetic Cause and the Predisposition to Renal Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1130 |
| Study Type | OBSERVATIONAL |
| Conditions | Renal Tumor Histology; Cutaneous Leiomyoma; Kidney Cancer |
This study will investigate what causes hereditary leiomyomatosis renal (kidney) cell cancer, or HLRCC, and how the disease is related to the development of kidney tumors. Leiomyomas are benign (non-cancerous) tumors arising from smooth muscle. HLRCC can cause various health problems. Some people develop red bumps on their skin that can be painful at times. Some women with HLRCC can develop lei…
NCT01087333 — Collection of Human Samples to Study Hairy Cell and Other Leukemias, and to Develop Recombinant Immunotoxins for Cancer Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1263 |
| Study Type | OBSERVATIONAL |
| Conditions | Hairy Cell Leukemia (HCL); Chronic Lymphocytic Leukemia (CLL); Non-Hodgkins Lymphoma (NHL); Cutaneous T Cell Lymphoma (CTCL); Adult T Cell Lymphoma (ATL) |
Background:
- Researchers who are studying hairy cell leukemia, and how the disease compares with other disorders, are interested in obtaining additional samples from leukemia patients and healthy volunteers. The investigators are particularly interested in samples from individuals who have diseases that can be treated with a new type of drug called immunotoxin, in which an antibody carrying …
NCT01109394 — Comprehensive Omics Analysis of Pediatric and Adult Solid Tumors and Establishment of a Repository for Related Biological Studies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6035 |
| Study Type | OBSERVATIONAL |
| Conditions | Sarcoma; Endocrine Tumors; Neuroblastoma; Retinoblastoma; Renal Cancer |
Background:
- Laboratory investigators who are studying common childhood cancers are interested in developing a tissue repository to collect and store blood, serum, tissue, urine, or tumors of children who have cancer or adults who have common childhood cancers. To develop this repository, additional samples will be collected from children and adults who have been diagnosed with common childh…
NCT03866382 — Testing the Effectiveness of Two Immunotherapy Drugs (Nivolumab and Ipilimumab) With One Anti-cancer Targeted Drug (Cabozantinib) for Rare Genitourinary Tumors
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 314 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder 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 …
NCT04616560 — Trastuzumab Deruxtecan (DS-8201a) for the Treatment of Newly Diagnosed, Recurrent or Refractory Osteosarcoma, Wilms Tumor, and Desmoplastic Small Round Cell Tumor
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 55 |
| Study Type | INTERVENTIONAL |
| Conditions | Desmoplastic Small Round Cell Tumor; Osteosarcoma; Recurrent Desmoplastic Small Round Cell Tumor; Recurrent Kidney Wilms Tumor; Recurrent Osteosarcoma |
| Interventions | ; ; |
This phase I/II trial studies the effects of trastuzumab deruxtecan (DS-8201a) in treating patients with osteosarcoma, Wilms tumor (WT) or desmoplastic small round cell tumor (DSRCT) that is newly diagnosed or has come back after a period of improvement (recurrent) or that has not responded to previous treatment (refractory). Trastuzumab deruxtecan is in a class of medications called antibody-d…
NCT04628767 — Testing the Addition of MEDI4736 (Durvalumab) to Chemotherapy Before Surgery for Patients With High-Grade Upper Urinary Tract Cancer
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 131 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Pelvis and Ureter Urothelial Carcinoma |
| Interventions | ; ; |
This phase II/III trial compares the effect of adding durvalumab to chemotherapy versus chemotherapy alone before surgery in treating patients with upper urinary tract cancer. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body’s immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Chemotherapy drugs, such as methotre…
NCT04981509 — Testing of Bevacizumab, Erlotinib, and Atezolizumab in Combination for Advanced-Stage Kidney Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 65 |
| Study Type | INTERVENTIONAL |
| Conditions | Hereditary Leiomyomatosis and Renal Cell Carcinoma; Papillary Renal Cell Carcinoma; Renal Cell Carcinoma; Sporadic Papillary Renal Cell Carcinoma; Stage III Renal Cell Cancer AJCC v8 |
| Interventions | ; ; |
This phase II trial studies the effects of combination therapy with bevacizumab, erlotinib, and atezolizumab in treating patients with hereditary leiomyomatosis and kidney cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Bevacizumab is in a class of medications called antiangiogenic agents. They work by stopping the …
NCT05334069 — Collecting Blood Samples From Patients With and Without Cancer to Evaluate Tests for Early Cancer Detection
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Alliance for Clinical Trials in Oncology |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute Lymphoblastic Leukemia; Acute Myeloid Leukemia; Ann Arbor Stage I Lymphoma; Ann Arbor Stage II Lymphoma; Ann Arbor Stage III Lymphoma |
| Interventions | ; |
This study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.
NCT05581004 — A Study to Evaluate the Safety, Pharmacokinetics, and Activity of Enzelkitug as a Single Agent and in Combination With Checkpoint Inhibitor in Participants With Locally Advanced or Metastatic Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Genentech, Inc. |
| Enrollment | 450 |
| Study Type | INTERVENTIONAL |
| Conditions | Locally Advanced or Metastatic Solid Tumors; NSCLC; HNSCC; Melanoma; TNBC |
| Interventions | ; ; |
This is a first-in-human study to evaluate the safety, tolerability, pharmacokinetics (PK), and anti-tumor activity of enzelkitug when administered as a single agent and in combination with atezolizumab or pembrolizumab in adult participants with locally advanced or metastatic solid tumors, including non small cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), melanoma, tr…
NCT04923178 — A Multi-Center Natural History of Urothelial Cancer and Rare Genitourinary Tract Malignancies
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1100 |
| Study Type | OBSERVATIONAL |
| Conditions | Urothelial Cancer; Bladder Cancer; Genitourinary Cancer; Urogenital Neoplasms; Urogenital Cancer |
Background:
Tumors in the genitourinary tracts can occur in the kidney, bladder, prostate, and testicles and can have common and rare histologies. Some cancers that occur along the genitourinary (GU) tract are rare. Some GU tumors are so rare that they are not included in treatment studies or tissue banks. This makes it hard for researchers to determine standards of care. Researchers want to l…
NCT05536141 — A Phase 1 Study of AB521 Monotherapy and Combination Therapies in Renal Cell Carcinoma and Other Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Arcus Biosciences, Inc. |
| Enrollment | 362 |
| Study Type | INTERVENTIONAL |
| Conditions | Clear Cell Renal Cell Carcinoma; Solid Tumors |
| Interventions | ; ; |
The purpose of this study is to evaluate the safety and tolerability of:
- casdatifan when taken alone in participants with advanced solid tumor malignancies and clear cell renal cell carcinoma (ccRCC) during the dose escalation stage; and
- casdatifan monotherapy and casdatifan in combination with cabozantinib or zimberelimab or zimberelimab and ipilimumab in participants with ccRCC in the do…
NCT05127824 — Autologous Dendritic Cell Vaccine in Kidney Cancer
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Jodi Maranchie |
| Enrollment | 42 |
| Study Type | INTERVENTIONAL |
| Conditions | Carcinoma, Renal Cell |
| Interventions | ; |
The purpose of this study is to estimate the probability of immune response for the combination treatment of dendritic cell vaccine with oral cabozantinib and characterize the safety profile of interventional therapy.
NCT06083922 — A Study of CyBorD (Cyclophosphamide, Bortezomib, Dexamethasone) Plus Daratumumab in People With Monoclonal Gammopathy of Renal Significance (MGRS)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma; Monoclonal Gammopathy of Renal Significance |
| Interventions | ; ; |
The purpose of this study is to find out whether cyclophosphamide, bortezomib, dexamethasone (CyBorD) with daratumumab SC is a safe treatment combination for MGRS-associated kidney disease including cast nephropathy associated with multiple myeloma. In addition, the researchers will find out whether the study drug combination is an effective treatment for these conditions.
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
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 992 |
| Study Type | INTERVENTIONAL |
| Conditions | Muscle 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…
NCT06465069 — A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 420 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Solid Tumor; Recurrent Solid Tumor; Advanced Solid Tumor; Urinary Bladder Neoplasm; Triple Negative Breast Cancer |
| Interventions |
The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approximately 4 years.
NCT06161532 — Sacituzumab Govitecan With or Without Atezolizumab Immunotherapy in Rare Genitourinary Tumors (SMART) Such as High Grade Neuroendocrine Carcinomas, Adenocarcinoma, and Squamous Cell Bladder/Urinary Tract Cancer, Renal Medullary Carcinoma and Penile C…
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Small Cell Carcinoma of the Bladder; Small Cell Carcinoma of the Urinary Tract; Squamous Cell Carcinoma of the Bladder; Squamous Cell Carcinoma of the Urinary Tract; Primary Adenocarcinoma of the Bladder |
| Interventions | ; |
Background:
Rare tumors of the genitourinary (GU) tract can appear in the kidney, bladder, ureters, and penis. Rare tumors are difficult to study because there are not enough people to conduct large trials for new treatments. Two drugs-sacituzumab govitecan (SG) and atezolizumab-are each approved to treat other cancers. Researchers want to find out if the two drugs used together can help peopl…
NCT06839105 — A Clinical Study to Evaluate the Safety and Tolerability of AWT020 in Patients With Advanced Malignancies
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Shanghai Junshi Bioscience Co., Ltd. |
| Enrollment | 214 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-Small Cell Lung Cancer, Colorectal Cancer, Renal Cell Carcinoma, Melanoma and Other Solid Tumor |
| Interventions | ; ; |
The purpose of this phase I clinical study was to evaluate the safety and tolerability of AWT020 monotherapy and combination with other antitumor therapies in patients with advanced malignancies
NCT06764771 — A Study of BMS-986488 as Monotherapy and Combination Therapy in Participants With Advanced Malignant Tumors
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Bristol-Myers Squibb |
| Enrollment | 437 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Malignant Tumors |
| Interventions | ; ; |
This purpose of this study is to determine if experimental treatment with BMS-986488, alone, or in combinations is safe, tolerable, and has anti-cancer activity in patients with advanced malignant tumors.
NCT07115043 — A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | AstraZeneca |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Melanoma; Non-small Cell Lung Cancer; Squamous Cell Carcinoma (Skin); Renal Cell Carcinoma; Merkel Cell Carcinoma |
| Interventions | ; |
A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors
NCT07011719 — Study of Casdatifan and Cabozantinib Versus Placebo and Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Arcus Biosciences, Inc. |
| Enrollment | 720 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Clear Cell Renal Cell Carcinoma; Advanced Clear Cell Renal Cell Carcinoma |
| Interventions | ; ; |
The purpose of the study is to evaluate the progression-free survival (PFS) of casdatifan versus placebo when each is given in combination with cabozantinib in adult patients with confirmed advanced or metastatic clear cell Renal Cell Carcinoma who have experienced progression on or after prior anti-PD-1 or anti-PD-L1 immunotherapy.
NCT07087158 — A Study of IBR854 Combined With Pazopanib Versus Pazopanib in Advanced Renal Cell Carcinoma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Imbioray (Hangzhou) Biomedicine Co., Ltd. |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Cell Carcinoma (RCC) |
| Interventions | ; |
This is a multicenter, randomized, open-label, active-controlled Phase II clinical study evaluating the efficacy and safety of IBR854 combined with Pazopanib versus Pazopanib in Advanced Renal Cell Carcinoma.
NCT07227402 — A Clinical Study of Belzutifan and Zanzalintinib in People With Recurrent Kidney Cancer Following Adjuvant Therapy (MK-6482-033)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 904 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Cell Carcinoma |
| Interventions | ; ; |
Researchers are looking for more ways to treat advanced renal cell carcinoma (RCC) that is recurrent. Researchers want to learn if recurrent advanced renal cell carcinoma (RCC) responds (gets smaller or goes away) after treatment with belzutifan (MK-6482) and zanzalintinib compared to cabozantinib.
The goal of this study is to learn if:
People who take belzutifan and zanzalintinib live longer…
NCT07227415 — Symbiotic-GU-08: A Study to Learn About the Medicine Called PF-08634404 Dosed Alone and in Combination With Other Anticancer Therapies in Adults With Locally Advanced or Metastatic Renal Cell Cancer
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Pfizer |
| Enrollment | 224 |
| Study Type | INTERVENTIONAL |
| Conditions | Carcinoma, Renal Cell; Advanced Renal Cell Carcinoma; Renal Cancer; Renal Neoplasm; Clear Cell Renal Cell Carcinoma |
| Interventions | ; ; |
This study is testing a new medicine called PF-08634404 and how it works in adults with advanced Renal Cell Carcinoma (RCC)- a type of kidney cancer that is either locally advanced (spread to nearby tissues) or metastatic (spread to other parts of the body). The study will look at the safety of the study medicine, when given alone or with other anticancer medicines, and how this type of cancer …
NCT07489495 — A Clinical Study of Belzutifan (MK-6482) and Zanzalintinib in People With Renal Cell Carcinoma (RCC) (LITESPARK-034/LS-034/MK-6482-034)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 758 |
| Study Type | INTERVENTIONAL |
| Conditions | Carcinoma, Renal Cell |
| Interventions | ; ; |
Researchers are looking for new ways to treat advanced renal cell carcinoma (RCC).
A standard (usual) treatment for certain people with RCC is belzutifan (a study medicine), which is a targeted therapy. Targeted therapy is a treatment that works to control how specific types of cancer cells grow and spread. Researchers want to learn if adding another targeted therapy called zanzalintinib (anot…
NCT07188896 — A Randomized Trial of Fianlimab and Cemiplimab +/- Ipilimumab or Ipilimumab Plus Nivolumab in First-line Advanced Renal Cell Carcinoma (RCC)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Brian Rini |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Renal Cell Carcinoma (aRCC); Metastatic Renal Cell Carcinoma ( mRCC); Clear Cell Renal Cell Carcinoma (ccRCC) |
| Interventions | ; ; |
This three-arm randomized phase 2 trial will enroll advanced clear cell RCC patients (all IMDC risk groups). Patients will be randomized 2:2:1 to either Arm A (fianlimab/ cemiplimab/ ipilimumab), Arm B (fianlimab/ cemiplimab), or Arm C (standard ipilimumab/ nivolumab), respectively.
NCT07688187 — A Study of Theranostic Pair PD-32766D/T in Participants With Carbonic Anhydrase IX Positive Clear Cell Renal Cell Carcinoma
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | PeptiDream Inc. |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Clear Cell Renal Cell Carcinoma |
| Interventions | ; |
This is an open-label, multicenter, Phase 1a/1b study evaluating the theranostic pair 64Cu-PD-32766 Injection (PD-32766D) and 225Ac-PD-32766 Injection (PD-32766T) in adult patients with relapsed or refractory Carbonic Anhydrase IX (CA9)-expressing clear cell renal cell carcinoma (ccRCC). The primary objective is to evaluate the safety and tolerability of PD-32766T, and to characterize its pharm…
NCT07611825 — Gut Microbiota Modulation for Immunotherapy Resensitization in Advanced Renal Cell Carcinoma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Jinling Hospital, China |
| Enrollment | 33 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced RCC |
| Interventions | ; |
The combination of immune checkpoint inhibitors (ICIs) and tyrosine kinase inhibitors (TKIs) has significantly improved clinical outcomes in patients with advanced renal cell carcinoma (RCC). However, 40%-60% of patients still develop primary or acquired resistance. For those with resistant disease, current immune rechallenge strategies have yet to demonstrate clear clinical benefit. Emerging e…
NCT07585760 — CM336 Plus Isatuximab for Newly Diagnosed Multiple Myeloma With Renal Impairment
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Institute of Hematology & Blood Diseases Hospital, China |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma (MM); Multiple Myeloma Light Chain Induced Renal Insufficiency |
| Interventions |
This study is a single-center, single-arm, open-label, Phase II interventional clinical trial designed to evaluate the efficacy and safety of a CM336 and isatuximab regimen in patients with newly diagnosed multiple myeloma (NDMM) accompanied by renal impairment ([eGFR] < 40 mL/min). Enrolled subjects will receive three consecutive cycles of induction therapy with CM336 in combination with is…
Active, Not Recruiting
NCT01582204 — Evaluate The Utility Of 124I-cG250 for The Early Detection Of Response to Therapy In Patients With Metastatic Renal Cell Carcinoma
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 17 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Cancer |
| Interventions |
Usually, doctors monitor kidney cancer with CT scans to measure the size of tumors. Sometimes, even when a drug is working, it can take several months before the effects are seen on a regular CT scan. The purpose of this study is to see if a new kind of scan, called 124I-cG250 PET/CT, can determine response to sunitinib or pazopanib earlier than a regular CT scan.
Research has shown that certa…
NCT01888198 — Ablation of Renal Masses Outcomes Registry (ARMOR): Ablation Procedure and Quality of Life Assessment
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Memorial Sloan Kettering Cancer Center |
| Enrollment | 294 |
| Study Type | OBSERVATIONAL |
| Conditions | Renal Cancer |
| Interventions | ; |
The purpose of this study is to better understand how effective ablation is for destroying tumor cells in the kidney and whether quality of life is improved for patients. Participation in ARMOR may involve retrospective data collection only, combined retrospective and prospective data collection, or prospective data collection
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT03055013 — Nivolumab in Treating Patients With Localized Kidney Cancer Undergoing Nephrectomy
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 819 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Renal Cell Carcinoma; Sarcomatoid Renal Cell Carcinoma; Stage II Renal Cell Cancer AJCC v7; Stage III Renal Cell Cancer AJCC v7; Unclassified Renal Cell Carcinoma |
| Interventions | ; ; |
This phase III trial compares nephrectomy (surgery to remove a kidney or part of a kidney) with nivolumab to the usual approach of nephrectomy followed by standard post-operative follow-up and monitoring, in treating patients with kidney cancer that is limited to a certain part of the body (localized). Nivolumab is a drug that may help stimulate the immune system to attack any cancer cells that…
NCT03244384 — Testing MK-3475 (Pembrolizumab) After Surgery for Localized Muscle-Invasive Bladder Cancer and Locally Advanced Urothelial Cancer
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 739 |
| Study Type | INTERVENTIONAL |
| Conditions | Localized Renal Pelvis and Ureter Urothelial Carcinoma; Locally Advanced Bladder Urothelial Carcinoma; Locally Advanced Renal Pelvis and Ureter Urothelial Carcinoma; Locally Advanced Ureter Urothelial Carcinoma; Locally Advanced Urothelial Carcinoma |
| Interventions | ; ; |
This phase III trial studies how well pembrolizumab works in treating patients with bladder cancer that has spread into the deep muscle of the bladder wall (muscle-invasive) or urothelial cancer that has spread from where it started to nearby tissue or lymph nodes (locally advanced). Monoclonal antibodies recognizing and blocking checkpoint molecules can enhance the patient’s immune response an…
NCT03595124 — A Study to Compare Treatments for a Type of Kidney Cancer Called TFE/Translocation Renal Cell Carcinoma (tRCC)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Metastatic Renal Cell Carcinoma; Stage III Renal Cell Cancer AJCC v8; Stage IV Renal Cell Cancer AJCC v8; TFE3-Rearranged Renal Cell Carcinoma; Unresectable Renal Cell Carcinoma |
| Interventions | ; |
This phase II trial studies how well axitinib and nivolumab work in treating patients with TFE/translocation renal cell carcinoma that cannot be removed by surgery (unresectable) or has spread to other places in the body (metastatic). Axitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as nivolumab, m…
NCT03793166 — Immunotherapy With Nivolumab and Ipilimumab Followed by Nivolumab or Nivolumab With Cabozantinib for Patients With Advanced Kidney Cancer, The PDIGREE Study
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1175 |
| Study Type | INTERVENTIONAL |
| Conditions | Clear Cell Renal Cell Carcinoma; Metastatic Malignant Neoplasm in the Bone; Metastatic Malignant Neoplasm in the Lymph Nodes; Metastatic Malignant Neoplasm in the Soft Tissue; Metastatic Malignant Neoplasm in the Viscera |
| Interventions | ; ; |
This phase III trial compares the usual treatment (treatment with ipilimumab and nivolumab followed by nivolumab alone) to treatment with ipilimumab and nivolumab, followed by nivolumab with cabozantinib in patients with untreated renal cell carcinoma that has spread to other parts of the body. The addition of cabozantinib to the usual treatment may make it work better. Immunotherapy with monoc…
NCT05220267 — Anlotinib Plus Sintilimab as First-line Treatment for Advanced Non Clear Cell Renal Cell Carcinoma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Sun Yat-sen University |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Non Clear Cell Renal Carcinoma |
| Interventions |
The combination of immune checkpoint inhibitors (ICIs) plus angiogenesis inhibitors has demonstrated significant anti-tumor activity in certain cancer. The goal of this study was to evaluate the efficacy and safety of sintilimab (a human programmed death-1 ICI) plus anlotinib (a multi-target tyrosine kinase inhibitor, inhibiting tumor angiogenesis and proliferative signaling) in advanced non cl…
NCT05614102 — A First-in-human Study to Learn How Safe the Study Drug BAY2965501 is, Find the Best Dose (Single Drug & Combination), How it Affects the Body, What Maximum Amount Can be Given, How it Moves Into, Through and Out of the Body, How it Acts on Different Tumors in Participants With Advanced Solid Tumors
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Bayer |
| Enrollment | 284 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Solid Tumors |
| Interventions | ; ; |
Researchers are looking for a better way to treat people who have advanced solid tumors. Advanced solid tumors are types of cancer that may have spread to nearby tissue, lymph nodes, and/or to distant parts of the body and that are unlikely to be cured or controlled with currently available treatments. This study focuses on certain types of skin cancer, kidney cancer, stomach cancer, and lung c…
NCT06147037 — A Phase 1, Dose-escalation Study of [225Ac]-FPI-2068 in Adult Patients With Advanced Solid Tumours
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | AstraZeneca |
| Enrollment | 13 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Solid Tumor; Metastatic Colorectal Carcinoma; Head and Neck Squamous Cell Carcinoma; Non-small Cell Lung Cancer; Pancreatic Ductal Adenocarcinoma |
| Interventions | ; ; |
This is a first-in-human, Phase 1, non-randomized, multicenter, open-label clinical study designed to investigate the safety, tolerability, dosimetry, biodistribution, and pharmacokinetics (PK) of [225Ac]-FPI-2068, [111In]-FPI-2107, and FPI-2053 in metastatic and/or recurrent solid tumors (HNSCC, NSCLC, mCRC, PDAC, GC, RCC).
Not Yet Recruiting
NCT07681817 — Risk Stratification and Proactive Nursing Intervention for Acute Kidney Injury Following Interventional Therapy in Patients With Liver Cancer
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Tianjin Medical University Cancer Institute and Hospital |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer, Adult |
| Interventions | ; |
This study focuses on the early identification and precision prevention of acute kidney injury (AKI) following interventional therapy in patients with liver cancer. A prospective, phased mixed-methods research design will be adopted. In the first phase, a prospective cohort study will be conducted to systematically collect clinical and nursing-related data. A Super Learner ensemble algorithm wi…
NCT07686744 — Neoantigen Peptide Vaccine Plus Pembrolizumab in Renal Cell Carcinoma
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Jian Lin |
| Enrollment | 8 |
| Study Type | INTERVENTIONAL |
| Conditions | Renal Cell Carcinoma; Advanced; Recurrent; Refractory |
| Interventions |
This is a Phase I, single-center, open-label, single-arm clinical trial to evaluate the safety and efficacy of personalized neoantigen polyepitope peptide vaccine combined with pembrolizumab in patients with advanced, recurrent or refractory renal cell carcinoma (RCC).
Background: Renal cell carcinoma is one of the most common malignancies of the urinary system. Although pembrolizumab has beco…
NCT07689812 — A Multicenter Randomized Open-Label Trial Evaluating MRD-Guided Interruption Versus Standard of Care Immune-Checkpoint Inhibitor (ICI) Therapy In Patients With Advanced / Metastatic Solid Tumors.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Natera, Inc. |
| Enrollment | 920 |
| Study Type | INTERVENTIONAL |
| Conditions | NSCLC (Advanced Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Cancer); NSCLC (Non-small Cell Lung Carcinoma); NSCLC; Melanoma (Skin Cancer) |
| Interventions |
This is an open-label, randomized study evaluating whether MRD-guided intermittent ICI therapy provides comparable survival to SOC continuous ICI therapy in subjects with histologically confirmed advanced / metastatic NSCLC, melanoma, MSI-High/dMMR CRC, RCC and other solid tumors. This study will be conducted in up to 100 sites.
NCT07689240 — Testing the Investigational Medication Pembrolizumab After Kidney Removal for Patients With Non-Clear Cell Renal Cell Carcinoma
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 400 |
| Study Type | INTERVENTIONAL |
| Conditions | Non-Clear Cell Renal Cell Carcinoma; Stage III Renal Cell Cancer AJCC v8; Stage IV Renal Cell Cancer AJCC v8 |
| Interventions | ; ; |
This phase III trial compares the effect of pembrolizumab to active surveillance after a surgical procedure to completely or partially remove a kidney (nephrectomy) in improving time without disease in patients with non-clear cell renal cell cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body’s immune system attack the cancer, and may interfere with the ab…
Enrolling by Invitation
NCT00102544 — Use of Tracking Devices to Locate Abnormalities During Invasive Procedures
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 3894 |
| Study Type | INTERVENTIONAL |
| Conditions | Adenocarcinoma; Prostate Neoplasms; Prostate Cancer; Renal Cell Carcinoma; Von Hippel Lindau Disease |
| Interventions |
This study will evaluate the accuracy and effectiveness of an experimental tracking device for locating abnormalities during invasive procedures, such as biopsy or ablation, that cannot easily be visualized by usual imaging techniques, such as computed tomography (CT) scans or ultrasound. Some lesions, such as certain liver or kidney tumors, small endocrine abnormalities, and others, may be har…
Completed Trials
NCT01352962 — Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Urethral Neoplasms; Neoplasms, Urethral; Cancer of the Urethra; Urethral Cancer |
| Interventions | ; ; |
Background:
- Gemcitabine and carboplatin are chemotherapy drugs used to treat several types of cancer, including cancer of the pancreas, bladder, ovaries, and lung. Lenalidomide, a drug that prevents the growth of new blood vessels in tumors, has been approved for treatment of certain blood cancers, but it has not yet been approved for use in combination with gemcitabine and carboplatin. Res…
NCT02964078 — Interleukin-2 and Pembrolizumab for Metastatic Kidney Cancer
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | H. Lee Moffitt Cancer Center and Research Institute |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Kidney Cancer |
| Interventions | ; |
The main purpose of this study is to evaluate the effects of the interleukin-2 given in combination with pembrolizumab.
Interleukin-2 (IL-2) is also called aldesleukin, or Proleukin™.
Pembrolizumab is also called Keytruda™, or anti-PD-1 antibody.
NCT03345563 — Project HERO: Health Empowerment & Recovery Outcomes
| Status | Completed |
| Phase | N/A |
| Sponsor | Rutgers, The State University of New Jersey |
| Enrollment | 113 |
| Study Type | INTERVENTIONAL |
| Conditions | Prostate Cancer; Bladder Cancer; Kidney Cancer; Colon Cancer; Rectum Cancer |
| Interventions | ; ; |
Project HERO is a 12-week study of the efficacy of Body Mind Training (BMT, i.e. Tai Chi and Qigong in this project) for reducing fatigue in male cancer survivors. This 3-arm randomized clinical trial will examine inflammatory biology and selected gene-expression pathways that are hypothesized to contribute to the intervention’s effect.
NCT04718584 — the Efficacy and Safety of LDP in Patients With Urinary and Male Genital Tumors
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Dragonboat Biopharmaceutical Company Limited |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Bladder Cancer; Renal Carcinoma; Advanced Penile Carcinoma |
| Interventions |
This is a single-arm,open, multicenter, phase II clinical study of the efficacy and safety of human anti-PD-L1 monoclonal antibody Injection (LDP) in the treatment of urinary and male genital tumors.
NCT04773951 — A Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of JS004 in Advanced Solid Tumors
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Shanghai Junshi Bioscience Co., Ltd. |
| Enrollment | 47 |
| Study Type | INTERVENTIONAL |
| Conditions | Melanoma; Renal Carcinoma; Urothelial Carcinoma |
| Interventions |
An open-label, dose-escalation, phase I clinical study to evaluate the safety and tolerability of JS004 injection in the patients with advanced solid tumors who have failure in standard of care and are unable to tolerate standard of care and/or have no available standard of care. The study is divided into screening period, treatment period, and follow-up period.
- Screening period: Subjects w…
Other (No longer available)
NCT03874455 — Tazemetostat Expanded Access Program for Adults With Solid Tumors
| Status | No longer available |
| Phase | N/A |
| Sponsor | Epizyme, Inc. |
| Enrollment | N/A |
| Study Type | EXPANDED_ACCESS |
| Conditions | Epithelioid Sarcoma (Ex-US Only); Spindle Cell Sarcoma; Sinonasal Carcinoma; Small Cell Carcinoma of the Ovary Hypercalcemic Type; Thoracic Sarcoma |
| Interventions |
Patients with a diagnosis listed under “conditions” below are eligible to be considered for the EAP. These conditions must be serious or life-threatening at the time of enrollment and appropriate, comparable, or satisfactory alternative treatments must have been tried without clinical success. Patients with conditions not listed under “conditions” below are not eligible for the tazemetostat EAP.