Clinical trials

318

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

Condition / disease
Location
Status: Recruiting

HERizon-Breast: A ctDNA-Guided Adaptive Study of Sequential Anti-HER2 Therapies and CNS Prophylaxis to Induce Long-Term Remission

Thie purpose of this study is to find out whether a personalized treatment approach-using a series of ctDNA tests along with standard imaging scans to help decide when to step up (escalate) or decrease (de-escalate) sequential treatments (given one after another)-combined with local therapies (which treat cancer in a specific part of the body) and treatments that prevent cancer from spreading to the central nervous system (CNS; including the brain and spinal cord) can result in long-lasting remission and possibly cure some participants with HER2+ metastatic breast cancer.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 7
Eligibility criteria

Male or female participants who are ≥18 years old with histologically confirmed... [+17]

Patients diagnosed with HER2+ breast cancer as per American Society of Clinical... [+18]

Status: Recruiting

A Study of Obecabtagene Autoleucel in People With B-cell Acute Lymphoblastic Leukemia

The researchers are doing this study to find out whether obecabtagene autoleucel (obe-cel) is an effective treatment for people with B-cell acute lymphoblastic leukemia (ALL) that is in complete remission (CR, meaning all signs of cancer are gone) with no measurable residual disease (MRD-negative, meaning there are no detectable cancer cells). Participants in this study will have received past treatment for their B-cell ALL, and their disease will be in MRD-negative CR for the first time (first MRD-negative CR).

Participants needed: 40
Trial details
Phase: Phase 2Age: 40+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 9
Eligibility criteria

Diagnosis of CD19+ B-cell ALL. [+19]

Burkitt's leukemia or lymphoma [+9]

Status: Recruiting

Registry for Bone Metastases

The purpose of this study is to learn more about symptomatic bone metastases. This study is an international patient registry of people with symptomatic bone metastases. A patient registry is a database - a collection of health information - about a group of people, and it is usually focused on a specific diagnosis or condition.

Participants needed: 500
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 7Duration: 10 Years
Eligibility criteria

Age ≥22 years [+3]

Age <22 years

Status: Recruiting

A Study Comparing Standard Treatments in People With Non-Muscle Invasive Bladder Cancer (NMIBC)

The purpose of this study is to compare the effectiveness of different FDA-approved/NCCN-recommended drug treatments for NMIBC. In particular, the FDA-approved drug nadofaragene firadenovec will be compared to usual care with other NCCN-recommended standard treatments for NMIBC (gemcitabine with or without docetaxel, mitomycin, re-treatment with BCG, or pembrolizumab).

Participants needed: 125
Trial details
Phase: Phase 3Age: 21+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 9
Eligibility criteria

21 years of age or older [+6]

Opting for treatment with radical cystectomy [+2]

Status: Recruiting

Observational Study of Bone Complications in People With Post-menopausal Breast Cancer Who Have Stopped Treatment With Denosumab and Aromatase Inhibitors

The purpose of this study to gather information about changes in the bones after stopping treatment with aromatase inhibitor/AI and denosumab. The study team will collect information from 5 standard clinic visits over the course of 24 months. The information will include information about participant health assessments, blood test results, and imaging results. After 24 months, participation in this study will be complete.

Participants needed: 100
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 7
Eligibility criteria

Women with confirmed diagnosis of breast cancer [+4]

Patients with history of osteoporosis prior to starting denosumab, based on prev... [+3]

Status: Recruiting

A Study of Romosozumab in People With Breast Cancer and Osteoporosis

The researchers are doing this study to see if romosozumab is effective at helping with bone formation in people with metastatic breast cancer (MBC) that has spread to the bones. All participants will have osteoporosis. The researchers will also look at bone breakdown (resorption) in participants and determine if romosozumab is a safe treatment for osteoporosis in people with MBC that has spread to the bones.

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 20, 2026Locations: 7
Eligibility criteria

≥18 years of age at the time of giving informed consent; [+2]

Prior therapy with a bone-modifying agent (intraveous bisphosphonates or subcuta... [+5]

Status: Not yet recruiting

A Study of Radiation Therapy and Cemiplimab With or Without Fianlimab In People With Bladder Cancer

The researchers are doing this study to find out whether stereotactic body radiation therapy (SBRT) in combination with immunotherapy (cemiplimab with or without fianlimab) before cystectomy is an effective and safe treatment for people with muscle-invasive bladder cancer (MIBC).

Participants needed: 44
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 18, 2026Locations: 7
Eligibility criteria

Age ≥ 18 years at the time of informed consent [+21]

Evidence of metastatic disease on standard staging CT and/or MR imaging [+47]

Status: Recruiting

A Study Comparing Music Therapy and Cognitive Behavioral Therapy for Anxiety in Cancer Survivors

The researchers are doing this study to compare how music therapy and cognitive behavioral therapy, given virtually, may be able to reduce anxiety in people who have had cancer. In addition, this study will see if certain factors affect how well participants respond to music therapy or cognitive behavioral therapy. For example, the researchers will see if personal characteristics (like age, sex, race, and education) and ways of thinking (like expectations of therapy) may affect how well participants respond.

Participants needed: 368
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 18, 2026Locations: 3
Eligibility criteria

English- or Spanish-speaking [+25]

Completed active cancer treatment (e.g., surgery, radiation, chemotherapy) less... [+18]

Status: Recruiting

Acupuncture for People Experiencing Period Loss Due to Chemotherapy

The purpose of this study is to find out whether it is practical (feasible) to use acupuncture to treat period loss (amenorrhea) caused by chemotherapy treatment in people with cancer. The researchers will look at how many participants enroll and complete the study. The researchers will also study how treatment with acupuncture affects the amount of time for the menstrual cycle to return and symptoms and quality of life related to amenorrhea.

Participants needed: 60
Trial details
Phase: Phase 2Age: 15-40Biological sex: FemaleType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 7
Eligibility criteria

English speaking woman between the ages of 15 and 40 [+9]

Had been pregnant or lactating within 3 months prior to enrollment [+4]

Status: Recruiting

A Study of Lung Cancer Risk

The researchers are doing this study to learn more about factors that may increase the risk of lung cancer in people who have never smoked. This information may help predict which people who have never smoked may be more likely to get lung cancer.

Participants needed: 500
Trial details
Age: 40-74Biological sex: AllType: ObservationalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 14, 2026Locations: 7
Eligibility criteria

Female at birth [+6]

Status: Recruiting

A Study of Fludarabine Dosing in Children and Young Adults With B-cell Acute Lymphoblastic Leukemia

The researchers are doing this study to find out whether PK-targeted fludarabine is an effective Lymphodepletion (LD) chemotherapy approach for people with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL) who will receive tisagenlecleucel CAR T-cell therapy. The researchers will compare PK-targeted fludarabine dosing with standard fludarabine dosing to see which treatment approach is more effective. The researchers will also look at whether PK-targeted fludarabine dosing is feasible (practical), the side effects of the study treatment, and how the study treatment affects people's quality of life. The researchers will measure quality of life by having participants complete questionnaires.

Participants needed: 65
Trial details
Phase: Phase 3Age: 1+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 5
Eligibility criteria

Patients with B-ALL and eligible to receive commercial tisagenlecleucel. [+9]

Have a known immediate or delayed hypersensitivity reaction or idiosyncrasy to t... [+4]

Status: Recruiting

A Study of Teclistamab and Mezigdomide in People With Multiple Myeloma

The researchers are doing this study to find out whether combining teclistamab and mezigdomide is a safe and effective treatment approach in people with relapsed/refractory multiple myeloma (MM).

Participants needed: 18
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 7
Eligibility criteria

Patients with relapsed or refractory multiple myeloma who have been treated with... [+27]

Prior treatment with a BCMA targeted bispecific antibody [+33]

Status: Recruiting

Gemcitabine and Oxaliplatin Chemotherapy With or Without a Floxuridine and Dexamethasone Pump in People With Cholangiocarcinoma That Cannot Be Removed With Surgery

This study will compare the safety and effects of HAI floxuridine and dexamethasone combined with the standard chemotherapy drugs gemcitabine and oxaliplatin (GemOx) with those of GemOx alone in people with untreated cholangiocarcinoma that cannot be removed with surgery. The researchers want to find out whether the study treatment works better than the standard chemotherapy to delay progression of disease. For the study treatment to be considered better than the standard treatment, the study treatment should increase the time until progression of disease by an average of 3 months, compared with the usual approach.

Participants needed: 164
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 11
Eligibility criteria

Age ≥18 years [+12]

Presence of distant metastatic disease. Patients will undergo radiographic evalu... [+12]

Status: Recruiting

A Study of Counseling Support for Cancer Survivors Age 65+

The purpose of this study is to find out if a psychotherapy method called brief behavioral activation (BBA) can improve depression, anxiety, and overall well-being and encourage healthy lifestyle behaviors in English- and Spanish-speaking Older Adult Cancer Survivors (OACS). BBA is a therapeutic technique that guides people to set goals and engage in enjoyable or rewarding activities as a way of changing behavior and reducing symptoms of depression. In this study, BBA will be given by telephone or videoconference (remotely).

Participants needed: 454
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 7
Eligibility criteria

As per self-report or medical record, ≥65 years old [+7]

As per PI determination, requires a higher level of care for current passive or... [+6]

Status: Recruiting

A Study of Cyclophosphamide, Methotrexate, Fluorouracil (CMF) for People With Breast Cancer

The purpose of this study is to find out if it is practical (feasible) to give dose-dense CMF (cyclophosphamide, methotrexate, and fluorouracil) in two standard chemotherapy regimens in people with breast cancer, age 70 and older.

Participants needed: 76
Trial details
Phase: Phase 2Age: 70+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 17, 2026Locations: 7
Eligibility criteria

Patients must have histologically confirmed adenocarcinoma of the breast confirm... [+12]

Stage IV breast cancer [+4]

Status: Recruiting

Study of 2141-V11 in People With Non-muscle Invasive Bladder Cancer That Did Not Respond to Standard Treatment

The purpose of this study is to test the safety of the study drug 2141-V11 in people whose NMIBC did not respond to standard treatment, and who will not have the standard surgical procedure to remove the bladder. The researchers will test different doses of 2141-V11 to see which dose is safest in people. The researchers will also do tests to see how the body absorbs, distributes, and gets rid of 2141-V11. This study is one of the first to test 2141-V11 in people, and the first to test 2141-V11 delivered through a catheter into the bladder.

Participants needed: 115
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 14, 2026Locations: 7
Eligibility criteria

High-grade (HG) NMIBC (HG Ta, CIS, and/or T1) of urothelial histology that is un... [+54]

History of or currently being treated for muscle-invasive (T2, T3, T4) locally-a... [+10]

Status: Recruiting

A Study of Blood Based Biomarkers for Pancreas Adenocarcinoma

The purpose of this study is to develop a minimally invasive test to diagnose pancreatic cancer at early stages of disease and monitor response to treatment.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 14, 2026Locations: 13
Eligibility criteria

Radiological, histological or cytological confirmed diagnosis of locally advance... [+25]

Prior chemotherapy or radiation therapy for pancreatic cancer within the last 3... [+21]

Status: Recruiting

Study of a Support Program for Quality of Life in Chinese Cancer Patients and Survivors

The purpose of this study is to evaluate different combinations of cancer education sessions, counseling sessions, and peer support meetings developed for Chinese cancer patients and survivors. The researchers will look at whether the combinations are practical and effective, and how they impact participants' quality of life.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 13, 2026Locations: 7
Eligibility criteria

Diagnosed with cancer (any type/stage) (per EMR for MSK patients or self-report... [+7]

Per PI determination, requires a higher level of care for current passive or act... [+5]

Status: Recruiting

DESCANSO, a Mental Health Intervention for Depression, Insomnia, and Fatigue Symptoms in Latino People With Cancer

The purpose of this study is to improve ways of providing mental health support to Spanish-speaking Latino participants who have cancer and experience depression, insomnia, and fatigue. Investigators will test a special mental health intervention called DESCANSO/REST (Depresión/Depressed Mood, Cansancio/Fatigue, and Sueño/Sleep). The intervention can be delivered through telehealth.

Participants needed: 125
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 12, 2026Locations: 7
Eligibility criteria

Mental health provider [+13]

History of comorbidities within the last 12 months associated with fatigue and p... [+2]

Status: Recruiting

A Study of CD8+ T Cell Imaging During Treatment in People With Non-Small Cell Lung Cancer

The purpose of this study to learn whether PET/CT (positron emission tomography/computed tomography) scans using an imaging agent (radiotracer) called zirconium Zr 89 crefmirlimab berdoxam is a safe and effective way to identify CD8+ T cells

Participants needed: 5
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 13, 2026Locations: 7
Eligibility criteria

Patient must be 18 years of age or older at the time of signing the informed con... [+5]

Pregnant or breastfeeding women [+1]

Status: Recruiting

A Study of CRD3874-SI in People With Solid Tumors

This study will test the safety of a study drug called CRD3874-SI. The researchers will test different doses of CRD3874-SI to find the highest dose that causes few or mild side effects in participants. After the researchers find the highest safe dose of CRD3874-SI, they will test that dose in new groups of participants to help them learn more about the side effects of the study drug and find out whether CRD3874-SI is an effective treatment for for patients with advanced or metastatic malignant solid tumors including sarcoma and Merkel Cell Carcinoma. (MCC), Head and neck squamous cell carcinoma (HNSCC), Adenoid cycstic carcinoma (ACC), Uveal Melanoma, Muscosal and Acral melanoma, and Non small cell lung cancer. The researchers will also look at how the body absorbs, distributes, and gets rid of CRD3874-SI, and the how the body and immune system respond to CRD3874-SI.

Participants needed: 81
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 13, 2026Locations: 7
Eligibility criteria

Male or female age ≥ 18 years at the time of informed consent. [+41]

Known prior severe hypersensitivity to an investigational product or any compone... [+33]

Status: Recruiting

A Study of Decreasing Radiation Therapy and Chemotherapy in People With Head and Neck Cancer

The purpose of this study is to test the treatment approach of de-escalated radiation and chemotherapy followed by a planned neck dissection surgery in people with head and neck cancer. The study will look at how effective the treatment approach is against participants' cancer.

Participants needed: 12
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 12, 2026Locations: 6
Eligibility criteria

Histologically confirmed diagnosis of SCC of the head and neck (excluding nasoph... [+19]

All nasopharyngeal, nasal cavity/paranasal sinus, oral cavity, salivary gland, t... [+13]

Status: Recruiting

PET/CT Imaging of Small Cell Lung Cancer Using 89Zr-DFO-SC16.56

The purpose of this study is to look at how safe 89Zr-DFO-SC16.56 is, and how it is processed by the body in people with small cell lung cancer.

Participants needed: 105
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 12, 2026Locations: 1
Eligibility criteria

Signed, informed consent [+19]

History of anaphylactic reaction to humanized or human antibodies [+9]

Status: Recruiting

Radiation Therapy Approaches for People With Prostate Cancer

The purpose of the study is to explore the best ways of giving radiation therapy to balance cancer control and treatment side effects.

Participants needed: 126
Trial details
Phase: Phase 2Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 12, 2026Locations: 7
Eligibility criteria

Non-metastatic prostate cancer. [+2]

None

Status: Not yet recruiting

A Study of Cemiplimab and Fianlimab in People With Nasopharyngeal Carcinoma

The purpose of this study is to find out whether cemiplimab, with or without fianlimab, is an effective treatment for advanced nasopharyngeal carcinoma (NPC), when given with standard chemotherapy drugs gemcitabine and cisplatin before standard chemoradiation.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Memorial Sloan Kettering Cancer CenterUpdated: Aug 11, 2026Locations: 7
Eligibility criteria

Age ≥ 18 [+12]

Prior head and neck radiation (Exceptions can be made if the overlap regions are... [+32]