Personalized Adoptive Cellular Therapy Targeting MDS Stem Cell Neoantigens (PACTN)

Status unconfirmed · Phase 1

Conditions studied: Myelodysplastic Syndromes

In brief

This study will evaluate the safety of autologous T cells that have been immunized ex vivo with patient-specific MDS stem cell neoantigens in patients with MDS.

Key facts

Study ID

NCT03258359

Run by

PersImmune, Inc

People needed

12

Starts

2018-01-01

Expected to finish

2020-12-01

Last updated by the study team

2020-03-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Confirmed diagnosis of MDS according to the French-American-British (FAB) criteria. Subjects with MDS must have intermediate, high, or very high risk IPSS-R scores and cytopenia of at least one lineage.
• Relapsed/refractory disease, or inadequate response to at least 6 cycles of hypomethylating (HMA) therapy or subjects who decline HMA therapy. Subjects must not have received any MDS or AML directed therapy for >28 days prior to receiving the study treatment.
• Subjects who have opted not to undergo allogeneic hematopoietic stem cell transplantation or for whom no donor is available and who are not deemed eligible for high intensity chemotherapy.
• Age >18 year at the time of obtaining informed consent, male or female.
• An Eastern Cooperative Oncology Grou (ECOG) performance status score of 0, 1, or 2.
• Adequate organ function.
• Seronegative test for HIV-1/2 and hepatitis C antibodies (HCV), and a negative test for Hepatitis B antigen (HBsAg). If hepatitis C antibody test is positive, then the subject must be tested for the presence of antigen by RT-PCR and be HCV RNA negative.
• Women of childbearing potential must have negative pregnancy test prior to initiating study treatment.
• Life expectancy >6 months at time of screening.
• Ability to adhere to the protocol requirements and study visit schedule.

You may not qualify if…

• Subjects who anticipate use of other investigational or non-investigational agents for the treatment of MDS during the study period, aside from a stable dose of erythropoietin stimulating agent started >8 weeks prior to screening for this study.
• Subjects who have received investigational agents, cytotoxic chemotherapy, or radiotherapy within 28 days prior to entering the study, or who have not recovered from AEs dur to agents administered more than 28 days earlier.
• Subjects who are less than 21 days from surgery or have insufficient recovery from surgical-related trauma or wound healing.
• Prior history of allogeneic hematopoietic stem cell transplantation.
• Current use of granulocyte colony-stimulating factory (G-CSF) or GM-CSF.
• History of major organ autoimmune disease.
• Concurrent immunosuppressive therapy. A stable dose of prednisone <10 mg daily or inhaled corticosteroids are allowed.
• Any form of primary immunodeficiency.
• Active bacillus tuberculosis (TB) or any other active or uncontrolled infection.
• Pior history of treated malignancy in the past 2 years. Subjects with non-melanoma skin cancer, localized prostate cancer, and carcinoma in situ of the breast of cervix are allowed.
• Impaired cardiac function.
• Pregnant women are excluded from this study as the proposed treatment has not been well studied in pregnant subjects.
• Any other medical or psychiatric disorders, or social situation, that would, in the investigator's opinion, place the subject at unacceptable risk if he/she participates in the study.

Where it is running

• University of California, San Diego — San Diego, California, United States

Full record on ClinicalTrials.gov

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