RAPA-501 Therapy of ALS Expanded Access Protocol

Purpose

RAPA-501-ALS is an Intermediate-Size Expanded Access Trial of RAPA-501 autologous hybrid TREG/Th2 T stem cells in patients living with amyotrophic lateral sclerosis (pwALS).

Condition

  • Amyotrophic Lateral Sclerosis

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Male or female patients ≥ 18 years of age. 2. Patients with sporadic or familial amyotrophic lateral sclerosis (ALS) diagnosed as laboratory-supported possible, probable, or definite according to World Federation of Neurology El Escorial Criteria. 3. Pulmonary slow vital capacity (SVC) 50% of predicted normal (as measured within three months prior to screening or at the time of screening). 4. Must have a source of autologous T cells potentially sufficient to manufacture RAPA-501 T stem cells, as defined by a peripheral CD3+ T cell count ≥ 500 cells per μl. 5. Patients who are taking riluzole (Rilutek), edaravone (Radicava), and/or sodium phenylbutyrate/taurursodial (Relyvrio) are eligible if taking the drug for at least 30 days prior to the screening visit. 6. Patients must be ≥ two (2) weeks removed from major surgery, or investigational therapy. 7. Patients must have no ongoing, unstable serious illness other than ALS, as determined by the Site Investigator. 8. Serum creatinine less than or equal to 2.0 mg/dL. 9. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 x upper limit of normal (ULN). 10. Bilirubin ≤ 1.5 (except if due to Gilbert's disease). 11. No history of abnormal bleeding tendency. 12. Voluntary written consent must be given before performance of any study related procedure not part of standard medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care. 13. Not enrolled in another interventional clinical trial or expanded access protocol and must have stopped taking other experimental drug(s) at least 2 weeks prior to screening.

Exclusion Criteria

  1. Active uncontrolled infection. 2. Hypertension not adequately controlled by ≤ 3 medications. 3. History of documented pulmonary embolus within 6 months of enrollment. 4. Clinically significant cardiac pathology, as defined by: myocardial infarction within 6 months prior to enrollment, Class III or IV heart failure according to NYHA, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. 5. HIV, hepatitis B, or hepatitis C seropositive. 6. Pregnant or breastfeeding subjects. 7. Subjects of childbearing age, or males who have a partner of childbearing potential, who are unwilling to practice contraception. 8. Subjects may be excluded at the Principal Investigator discretion or if it is deemed that allowing participation would represent an unacceptable medical or psychiatric risk.

Study Design

Phase
Study Type
Expanded Access

Recruiting Locations

Barrow Neurological Institute
Phoenix, Arizona 85013

Mayo Clinic Hospital Phoenix
Scottsdale, Arizona 85259
Contact:
Megan Hall, M.S.N., R.N.
480-301-6373
Hall.Megan@mayo.edu

University of California Irvine Health
Irvine, California 92868
Contact:
UCI Alpha Clinic
949-824-3990
alphaclinic@hs.uci.edu

University of California, San Francisco
San Francisco, California 94143
Contact:
415-501-0671
Neuromuscular.Research@ucsf.edu

Emory University
Atlanta, Georgia 30322
Contact:
Anna Partlow, R.N., M.S.N.
anna.partlow@emory.edu

University of Iowa Health Care
Iowa City, Iowa 52242
Contact:
Emily Anderson, R.N., M.S.N.
319-356-8744
emily-anderson@uiowa.edu

Massachusetts General Hospital
Boston, Massachusetts 02114
Contact:
Megan Okoro
617-643-6252
mokoro@mgh.harvard.edu

University of Minnesota
Minneapolis, Minnesota 55455
Contact:
Julia Munoz
612-624-9987
munoz156@umn.edu

Hackensack University Medical Center
Hackensack, New Jersey 07601
Contact:
Andrew McConnell
551-996-5900
Andrew.McConnell@hmhn.org

Providence Portland Medical Center
Portland, Oregon 97213
Contact:
Ashley Adamo
503-962-1171
Ashley.adamo@providence.org

More Details

NCT ID
NCT06169176
Status
Available
Sponsor
Rapa Therapeutics LLC

Study Contact

Daniel H Fowler, M.D.; Chief Medical Officer, Rapa Therapeutics
301-518-3104
dan@rapatherapeutics.com

Detailed Description

ALS is a rare disease that is considered an orphan disease according to the Orphan Drug Act. This is an open-label, non-randomized, multi-center intermediate size expanded access clinical trial of single-agent RAPA-501 T stem cells in patients with high-risk ALS who are not eligible for other ALS clinical trials. After a subject consents to the study, an apheresis procedure will be performed to collect cells to manufacture the investigational product, RAPA-501 T stem cells. RAPA-501 cells are manufactured ex vivo using epigenetic reprogramming to yield a T stem cell population that is enriched for a dual anti-inflammatory phenotype based on hybrid TREG and Th2 differentiation. RAPA-501 T stem cells express both the TREG and Th2 transcription factors FOXP3 and GATA3, are enriched for expression of the ATP ectonucleotidase molecules CD39 and CD73, are enriched for the T cell homing molecule CD103, and suppress both effector T cell inflammatory molecules and CNS microglial cell inflammatory molecules. This study is evaluating RAPA-501 T stem cell therapy at the dose of 80 x 10EE6 cells per infusion, with up to 4 infusions separated by six weeks between doses (infusion at time 0, and then after week 6, 12, and 18). Study subjects are then followed for several months to capture major clinical events and to assess survival. The total duration of RAPA-501 T stem cell therapy and follow-up interval on this protocol is approximately 8-months (250 days). The primary objective in the expanded access cohort is to determine the feasibility and safety of the highest-dose established safe dose of RAPA-501 (80 x 10EE6 cells per infusion). Secondary study objectives relate to assessment of overall survival compared to historical controls and determining the ALS disease activity pre-therapy, during study interventions, and throughout the post-therapy observation interval of RAPA-501 therapy through the monitoring of ALSFRS-R scores, SVC values, hand grip strength, and ROADS Scale. In addition, secondary study objectives relate to characterizing immune system parameters pre- and post- therapy and the potential effect of RAPA-501 therapy on serum markers of neurodegeneration.