A Phase II Study of Neovii Anti-human T-lymphocyte Immunoglobulin (ATLG, Grafalon®) With Post Transplant Escalated Doses of Post-transplant-Cyclophosphamide to Prevent Acute and Chronic GVHD Post Allogeneic Stem Cell Transplantation

Who is this study for? Patients with Graft versus Host Disease
What treatments are being studied? Cyclophosphamide+Anti-Human T-Lymphocyte Immunoglobulin (ATLG)
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Investigators hypothesize that combination of ATLG with PTCy in matched or mismatched unrelated hematopoietic stem cell transplantation will reduce acute and chronic GVHD incidence. Furthermore it will allow shortening of the length of post-transplantation immunosuppression with calcineurin inhibitor (CNI) administration (currently administrated in addition to ATG as GVHD prophylaxis in daily common practice)

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with MDS/AML

• 18 years or older and willing and able to comply with the protocol requirements.

• LVEF ≥ 40%. 2-D transthoracic echocardiogram (ECHO) is the preferred method of evaluation. Multigated Acquisition Scan (MUGA) is acceptable if ECHO is not available.

• Patients undergoing 8-10/10 HLA matched unrelated and unmanipulated PBSC transplantation

• Patients conditioned with reduced intensity or reduced toxicity conditioning of fludarabine with reduced dose (2 days) or myeloabalative doses (4 days) of busulfan or with treosulfan.

• Patients must sign written informed consent.

• Adequate birth control in fertile patients.

Locations
Other Locations
Israel
Chaim Sheba Medical Center
RECRUITING
Ramat Gan
Contact Information
Primary
Arnon Nagler, MD
Arnon.Nagler@sheba.health.gov.il
972-3-530-58-30
Backup
Avichai Shimoni, MD
ashimoni@sheba.health.gov.il
Time Frame
Start Date: 2018-09-06
Estimated Completion Date: 2024-12-01
Participants
Target number of participants: 30
Treatments
Experimental: cyclophosphamide and ATLG
The study will include 2 phases. In the first phase escalated doses of post-transplant cyclophosphamide up to a maximal dose of 50 mg/kg administered on day +3 and +4 (target dose) will be added to a standard GVHD prophylaxis consisting of anti-human T-lymphocyte immunoglobulin (ATLG, Grafalon®, formerly ATG-Fresenius S, Neovii Pharmaceuticals) 15mg/kg total (5mg/kg day) on days -3 to -1 pre transplantation in order to find the maximally tolerated dose (MTD) of post-transplant cyclophosphamide (PTCy) in combination with pre-transplant immunosuppression by ATLG. The second phase will use the MTD cyclophosphamide dose identified in the first phase.
Sponsors
Leads: Sheba Medical Center

This content was sourced from clinicaltrials.gov

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