Clinical Specimen Collection From Pompe Disease Patients

Sponsor

Serhat Gumrukcu, MD PhD (Other)

Overall Status

Recruiting

CT.gov ID

NCT04476550

Collaborator

Frida Therapeutics LLC (Other)

Enrollment

Location

8.9

Anticipated Duration (Months)

1.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Clinical specimens are required from individuals with Pompe Disease to support process and analytical development for a genetically modified autologous bone marrow cell product currently in preclinical research, FTX-PD01. The intent is for this product to be investigated in a subsequent clinical trial under a future FDA IND to treat Pompe Disease. Enrolled participants provide a venous blood specimen (approximately 20mL) to be used in preclinical studies and research and development of FTX-PD01. Subjects may eventually be asked to undergo mobilized leukapheresis for bone marrow stem cell collection and their specimens will be used to further develop the FTX-PD01 cell product, including a cGMP compliant process to be applied under the future FDA IND.

Condition or Disease	Intervention/Treatment	Phase
Pompe Disease	Drug: Filgrastim

Detailed Description

This protocol is to collect blood and HSPC specimens from individuals with Pompe Disease. The first blood draw will be done at the first study visit and if eligible, the second collection will be done via mobilized leukapheresis at the second visit. The mobilized leukapheresis procedures will follow the facility's standard operating procedures and protocol requirements for mobilized leukapheresis.

Donors will be males or females between and including the ages of 3 years and 30 years. Volunteers will provide written informed consent and meet all inclusion and exclusion criteria. Each participant can be in the study for up to 120 days (3 months).

The study will be conducted in accordance with human research for the purposes of obtaining clinical specimens for research. There is no endpoint for this study, however, data collected from this study will include, but not be limited to, gender, demographics, medical history, clinical laboratory values, and volume of the blood collected. The data will be summarized in future studies reporting results from a future clinical trial under FDA IND.

Study Design

Study Type:

Observational

Anticipated Enrollment :

12 participants

Observational Model:

Case-Only

Time Perspective:

Prospective

Official Title:

Developing a Potential Cure for Pompe Disease: Clinical Specimen Collection From Individuals With Pompe Disease

Anticipated Study Start Date :

Sep 1, 2022

Anticipated Primary Completion Date :

Mar 1, 2023

Anticipated Study Completion Date :

May 31, 2023

Outcome Measures

Primary Outcome Measures

Collection of blood [Up to 20 days]
Collection of peripheral blood (up to 20ml)

Secondary Outcome Measures

Collection of HSPCs [Up to 100 days]
Collection of HSPCs through G-CSF mobilized leukapheresis

Eligibility Criteria

Criteria

Ages Eligible for Study:

3 Years to 30 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male of female aged 3-30
Documented diagnosis of Pompe Disease
Participants who has not participated in a cell or gene therapy trial for Pompe Disease

Exclusion Criteria:

Active acute infection at screening
Uncontrolled diabetes
Uncontrolled hypertension
Active DIC, bleeding or coagulopathy which cannot be corrected with minimal intervention
Symptomatic, uncontrolled or severe intercurrent illness that would compromise the ability to tolerate blood collection or mobilized leukapheresis procedure
Systemic chemotherapy less than or equal to 2 weeks (6 weeks for clofarabine or nitrosoureas) or radiation therapy less than or equal to 3 weeks prior to leukapheresis
Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test at screening
Any patient that in the opinion of the investigator is not medically stable to undergo the leukapheresis procedure or will not comply with the visit schedules or procedures