Clinical trials

9

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Condition / disease
Location
Status: Recruiting

The ECOG-ACRIN SUPPORT Trial: Multilevel Intervention to Improve Diverse Enrollment in Cancer Clinical Trials

The purpose of this study is to conduct a Hybrid Type 1 cluster-randomized, roll-out effectiveness-implementation trial in NCORP community oncology practice sites (N= 500 Black and Latino cancer patients) to evaluate the effectiveness of the EA SUPPORT intervention combining CT navigators and CT research literacy tools in improving Black and Latino patient referral and accrual to NCI-supported CTs (primary outcomes) and participant and provider awareness and knowledge of CTs (secondary outcomes) while assessing implementation factors. Also, with the CUSP2CT data, Evaluation, and Coordinating Center, conduct final site evaluation and disseminate the SUPPORT intervention to NCORP community oncology sites, research bases, and affiliated trial networks.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Testing Whether High Dose Chemotherapy and Infusion of the Patients' Own Stem Cells Improves Survival in Patients With Peripheral T-cell Lymphoma Who Achieved a Complete Response at the End of the Initial Chemotherapy

This phase III trial compares the effect of high dose chemotherapy and the patients' own (autologous) stem cells to observation only in patients with peripheral T-cell lymphoma who achieved a complete response after initial chemotherapy. Usual treatment after a complete response may include observation or high dose chemotherapy followed by an autologous stem cell transplant, however, it is not known if a transplant if beneficial. Giving chemotherapy before a stem cell transplant helps kill cancer cells in the body and helps make room in the patient's bone marrow for new blood-forming cells (stem cells) to grow. Stem cells removed prior to treatment are then returned to the patient to replace the blood forming cells that were destroyed by the chemotherapy. Giving high dose chemotherapy followed by an autologous stem cell transplant may be more effective compared to observation only in treating patients with peripheral T-cell lymphoma who have achieved a complete response after initial chemotherapy.

Participants needed: 294
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jun 18, 2026Locations: 158
Eligibility criteria

Patient must be 18 to 75 years of age [+22]

Status: Recruiting

Daratumumab for Chemotherapy-Refractory Minimal Residual Disease in T Cell ALL

In this study, the investigators are hypothesizing that daratumumab-hyaluronidase will effectively treat T-ALL in patients who have persistent or recurrent MRD following treatment with chemotherapy.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Patient must have documented T cell ALL and must be in first or later hematologi... [+19]

Status: Recruiting

Improving Adolescent and Young Adult Self-Reported Data in ECOG-ACRIN Trials

The purpose of this study is to evaluate feasibility and acceptability of completing PROs among AYAs randomized to Choice PRO vs Fixed PRO.

Participants needed: 400
Trial details
Age: 18-39Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jun 18, 2026Locations: 347
Eligibility criteria

Not listed

Status: Not yet recruiting

A Randomized Phase III Study of Management of Treatment Naive Primary Melanoma in Elderly Patients

Can we treat your melanoma just as effectively without doing a sentinel lymph node (SLN) biopsy in addition to your wide local excision (WLE) procedure? A wide local excision (WLE) is a surgical procedure performed to cut out an abnormal lesion and some surrounding normal tissue. This is sometimes followed by a sentinel lymph node (SLN) biopsy, in which lymph nodes that cancer cells could spread to are removed as well. We are doing this study because we want to find out if performing the WLE alone is just as effective as the usual approach for your melanoma, and if it leads to improvements in patients' overall well-being. The usual approach is defined as care most people get for the early stage of melanoma that you currently have.

Participants needed: 428
Trial details
Phase: Phase 3Age: 75+Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Nov 13, 2025Locations: 1
Eligibility criteria

Patient must be ≥ 75 years of age. [+6]

Patient must not have an active infection that precludes enrollment to this stud... [+3]

Status: Not yet recruiting

A Targeted Electronic Health Approach to Reduce Fear of Recurrence in Breast Cancer Survivors (FoRtitude)

The goal of this study is to determine if the intervention or if general information about being a breast cancer survivor can help Breast Cancer Survivors reduce their fear of recurrence. The main question it aims to answer are: Can the FoRtitude intervention lower the fear of recurrence for Breast Cancer Survivors? Participants will: Answer questions about their fear of recurrence. Be randomized to 1 of the 3 following options: (1) a weblink to access an eHealth intervention which includes a website and an optional interactive text-messaging feature, (2) a weblink to a non-interactive website that will include links to external websites with general information that may be helpful for Breast Cancer Survivors, or (3) you will need to talk with your oncology team about your concerns about recurrence or seek psychosocial care in the community. Be asked to fill out questionnaires 5 times for up to 18 months.

Participants needed: 800
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Aug 14, 2025Locations: 1
Eligibility criteria

Participant must be ≥ 18 years of age. [+10]

Participant must not have any psychiatric or cognitive conditions that may affec...

Status: Not yet recruiting

Testing the Effect of Sulforaphane, a Compound Naturally Found in Cruciferous Vegetables, on Preventing Melanoma in Patients With a Prior History of Melanoma

The goal of this clinical trial is to compare the safety and effects of sulforaphane with the safety and effects of placebo on people's risk of developing melanoma. The main question it aims to answer is: Will giving sulforaphane (a broccoli sprout extract) have a meaningful effect on how your atypical moles change over time? If there is an effect, will this lower your risk of developing melanoma? Participants will: Take sulforaphane or a placebo for 12 months Visit the clinic once every 3 months for checkups and tests You will keep a calendar which will help you keep track of when you take your tablets

Participants needed: 120
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jun 27, 2025Locations: 1
Eligibility criteria

Patient must have ≥ 3 clinically atypical nevi, assessed within 30 days prior to... [+11]

Patient must not be pregnant. [+3]

Status: Not yet recruiting

Extended Clinical Follow up and Biospecimen Collection for Patients Enrolled in TAILORx and RxPONDER: A Companion Protocol

The purpose of this study is to retrieve tissue samples from individuals with breast cancer who previously enrolled on the PACCT-1 (TAILORx) or S1007 (RxPONDER) trials and experiences a recurrence of their cancer (Cohort 1, 2, and 3), and/or the tumor initially removed at surgery in patients previously enrolled in step 1 of S1007 (RxPONDER) and found to have a high Recurrence Score of 26-100 (Cohort 3) but not followed on the study after that point. The tissue will be used for future research designed to understand why breast cancer recurs despite hormonal therapy or chemotherapy plus hormonal therapy.

Participants needed: 600
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Eastern Cooperative Oncology GroupUpdated: May 30, 2025
Eligibility criteria

Cohort 1: Previously enrolled on TAILORx (PACCT-1) with recurrence score (RS) 0-... [+5]

Status: Not yet recruiting

Testing the Use of Combination Therapy in Patients With Persistent Low Level Acute Myeloid Leukemia (AML) Following Initial Treatment

ERASE is part of the MyeloMATCH initiative, Young Adult Basket and is a Tier 2 study. The study is comparing the use of Cytarabine to Cytarabine and Venetoclax, Daunorubicin/Cytarabine Liposome and Venetoclax, and Azacitidine and Venetoclax.

Participants needed: 184
Trial details
Phase: Phase 2Age: 18-59Biological sex: AllType: InterventionalSponsor: Eastern Cooperative Oncology GroupUpdated: Jul 3, 2024
Eligibility criteria

Patient must be ≥ 18 and ≤ 59 years of age. [+11]

Patient must not be pregnant or breast-feeding due to the potential harm to an u... [+5]