SURPASS-3 STUDY/ GOG-3084

  • Research type

    Research Study

  • Full title

    A PHASE 2, OPEN-LABEL, RANDOMIZED, NON-COMPARATIVE CLINICALTRIAL OF ADP-A2M4CD8 MONOTHERAPY AND IN COMBINATION WITH NIVOLUMAB IN SUBJECTS WITH RECURRENT OVARIAN CANCERS (SURPASS-3 STUDY/ GOG-3084)

  • IRAS ID

    1007284

  • Contact name

    Eric Dollins

  • Contact email

    eric.dollins@adaptimmune.com

  • Sponsor organisation

    Adaptimmune LLC

  • Eudract number

    2022-003176-16

  • Clinicaltrials.gov Identifier

    NCT05601752

  • Research summary

    ADP-0055-003 is a clinical trial to evaluate if Adaptimmune T-cell therapy, ADP-A2M4CD8 works in ovarian cancer and is safe. ADP-A2M4CD8 is the patient's changed immune cells (T-cells) to target and attack cancer cells. Patients will receive ADP-A2M4CD8 with or without nivolumab. Patients are selected at random (by chance) to receive Nivolumab. Nivolumab is approved in various cancers.

    Patients with ovarian cancer are typically treated with surgery and chemotherapy. Some will receive chemotherapy alone. After receiving the first treatment, ovarian cancer usually returns in about 80% of patients. There is a need for effective ovarian cancer treatments.

    Patients will enrol into this clinical trial after chemotherapy has stopped working for them.
    One study using ADP-A2M4CD8 has shown benefit in ovarian cancer. In this study, patients will be assessed to determine which treatment: ADP-A2M4CD8 alone or a combination of nivolumab + ADP-A2M4CD8, shows a better benefit for patients with recurrent ovarian cancer. The safety of both treatments will be monitored and assessed to ensure that they have an acceptable risk.

  • REC name

    London - West London & GTAC Research Ethics Committee

  • REC reference

    23/LO/0629

  • Date of REC Opinion

    17 Oct 2023

  • REC opinion

    Further Information Favourable Opinion