PTCY Plus uhCG/EGF for Graft Versus Host Disease Prophylaxis
This study is testing a new way to prevent Graft Versus Host Disease (GVHD) after a stem cell transplant. GVHD is a complication where the new immune cells attack the patient's body. Researchers are combining two existing treatments: post-transplant cyclophosphamide (PTCY) and a mix of urinary-derived human chorionic gonadotropin and epidermal growth factor (uhCG/EGF). The main goal is to see if this combination is safe and feasible. You might be able to join if you are 18-70 years old, have a blood cancer requiring a stem cell transplant, and meet certain health requirements for your kidneys and liver. The study is also looking at how well it prevents GVHD and improves survival. The current recruitment status is unclear.
- Study design
- This is a Phase 1 interventional study with a planned enrollment of 18 participants. It is designed to evaluate the safety and feasibility of the treatment combination.
- What's involved
- You would receive PTCY for two doses after your stem cell transplant, followed by uhCG/EGF injections under the skin on days 7, 9, and 11 after your transplant. Safety will be measured up to 30 days after the stem cell transplant.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoints for safety and dose-limiting toxicity are measured at day +30 post stem cell transplant.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
PTCY Plus uhCG/EGF for Graft Versus Host Disease Prophylaxis
At a glance
Conditions
NCT04886726
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Henry Ford Hospital
Detroit, Michiganstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- MTDday+30 post SCT
The maximum tolerated dose
- Incidence and severity of dose limiting toxicity (DLTs)day+30 post SCT
The overall incidence and severity of DLTs for uhCG/EGF