| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| MICRO GI FEASIBILITY | 25-63 | People with endometrial cancer who are planned to receive external-beam radiotherapy as part of their cancer treatment. |
The MICRO-GI study aims to find out whether it is practical and acceptable for women receiving pelvic radiotherapy for endometrial cancer to take daily probiotic supplements and receive personalised dietary counselling. |
DSSG Group: Gynaecological
D8991C00002: Drug-drug Interaction Study With AZD5335 and Itraconazole in Participants With Ovarian, Primary Peritoneal, or Fallopian Tube Cancer
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| D8991C00002: Drug-drug Interaction Study With AZD5335 and Itraconazole in Participants With Ovarian, Primary Peritoneal, or Fallopian Tube Cancer | 26-35 | Ovarian, peritoneal, or fallopian tube cancer |
The purpose of this trial is to learn how safe AZD5335 is and if a drug called itraconazole changes how AZD5335 moves through the body over time in adults with ovarian, peritoneal, or fallopian tube cancer |
ENGOT cx22 Trofuse-036
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| ENGOT cx22 Trofuse-036 | 25-37 | Cervical cancer that has returned or spread to other parts of the body after treatment and is not treatable by surgery and/or radiation |
The purpose of this study is to learn: About the safety of sac-TMT with pembrolizumab and bevacizumab, and if people tolerate them when given together, and |
ENGOT OV-84 Trofuse-022
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| ENGOT OV-84 Trofuse-022 | 24-41 | Platinum-Sensitive Recurrent Ovarian Cancer and who have progressed after first line platinum-based therapy and have not progressed after second-line maintenance treatment. |
The trial is testing the efficacy of the investigational drug “Sacituzumab Tirumotecan (MK-2870)” during maintenance treatment, with or without Bevacizumab, compared to Standard of Care treatment. |
ENGOT en29 Trofuse-033
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| ENGOT en29 Trofuse-033 | 25-17 | Primary advanced or returned Endometrial cancer whose mismatch repair system is working normally and who are starting their first maintenance treatment. |
The trial is testing a new combination of treatments for people with advanced or recurring Endometrial Cancer whose cancer has a “normal” mismatch-repair system (so-called “mismatch repair proficient” or pMMR). |
Catalina-2 (ENGOT-ov83)
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| Catalina-2 (ENGOT-ov83) | 24-68 | Advanced Platinum-Resistant Epithelial Ovarian Cancer (Including Primary Peritoneal and Fallopian Tube Cancers) Expressing Claudin 6 |
The purpose of the study is to assess the efficacy of TORL-1-23 administered as monotherapy in women with advanced, platinum-resistant ovarian cancer whose tumors express the claudin-6 (CLDN6) biomarker. The study will also evaluate the overall safety and tolerability of TORL-1-23 and its potential therapeutic effects in this patient population |
Vulval Cancer: A Focus on Survivorship
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| Vulval Cancer: A Focus on Survivorship | 25-40 | Vulvar Cancer |
This research aims to understand the long-term impact of vulvar cancer and its treatments on various aspects of a woman’s life, including physical health, emotional well-being, and sexual functioning. |
RAMP-301 (ENGOT ov81)
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| RAMP-301 (ENGOT ov81) | 25-16 | Recurrent (previously treated) low grade serous ovarian cancer (LGSOC) who have progressed on a prior platinum-based therapy |
The purpose of the study is to assess how avutometinib plus defactinib compares to the standard |
HELP-ER
| Name | No. | For Patients with | Purpose |
|---|---|---|---|
| HELP-ER | 22-05 | First platinum sensitive relapsed ovarian cancer |
Prospective Study of HE4 serum Level in Patients with First Relapsed Ovarian Cancer. Improving the prediction of surgical outcome at secondary cytoreduction in patients with ovarian cancer. This study aims to improve upon the contemporary AGO score by including additional clinical variables like circulating HE4 and CA125 levels to predict surgical outcome at secondary cytoreduction. |
