CD19- and CD22-directed CAR-T Cell Therapy in Patients With Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia Clinical Trial

Official title:

Phase I, Open Label, Multicenter, Dose Escalation and Expansion Study of IMJ995 in Acute Lymphoblastic Leukemia

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT05168748
• Other study ID #: CIMJ995A12101
• Secondary ID: 2021-000677-89
• Status: Withdrawn
• Phase: Phase 1
• Start date: January 24, 2023
• Est. completion date: August 13, 2026

Study information

• Verified date: September 2022
• Source: Novartis
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a first-in-human study to evaluate the feasibility, safety and preliminary antitumor efficacy of autologous chimeric antigen receptor (CAR) T cells targeting both CD19 and CD22, manufactured with T-Charge(TM) process. CAR-T cells will be investigated as single agent in pediatric and adult acute lymphoblastic leukemia (ALL).

Description:

This is a phase I, open label, multicenter, dose escalation and expansion study of IMJ995. The study will investigate single agent IMJ995 in two independent groups of acute lymphoblastic leukemia (ALL) patients: - Pediatric, adolescent and young adult (AYA) ALL patients up to 29 years old - Adult ALL patients (≥30 years old) safety cohort The pediatric and AYA ALL group consists of two parts: a dose escalation part to evaluate feasibility, characterize safety and identify the recommended dose (RD) of IMJ995, and a dose expansion part to further characterize safety, cellular kinetics and assess preliminary antitumor activity. Once the RD of IMJ995 is determined for this group, the corresponding expansion part may commence. Once the RD of IMJ995 is determined for the pediatric and AYA group, a safety cohort for adult ALL patients ≥30 years old may commence in parallel to the above mentioned expansion part.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: August 13, 2026
• Est. primary completion date: August 13, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year and older

Eligibility

Inclusion Criteria:

All patients:

• Evidence of CD19 and/or CD22 cell surface expression on B-ALL blasts in bone marrow or peripheral blood by flow cytometry at time of relapse or prior to study entry.

Pediatric, adolescent and young adult ALL patients:

• 1 - 29 years of age at the time of informed consent form (ICF) signature.
• Relapsed or refractory CD19+ and/or CD22+ ALL after 3 or more lines of treatment OR after allogeneic HCT.
• Must have received a CD19-directed CAR-T treatment (with or without blinatumomab), unless prior loss of CD19 cell surface expression occurred or have not been eligible for CD19 directed CAR-T treatment.
• Lansky (age < 16 years), Karnofsky (age 16-25 years) performance status = 60%. ECOG (age >25 years) performance status that is either 0 or 1 at screening.

Adult ALL patients aged =30 years:

• =30 years of age at the time of informed consent form (ICF) signature.
• Refractory or relapsed CD19+ and/or CD22+ ALL including at least one of the following:
• After allogeneic HCT
• After 2 or more lines of treatment, including blinatumomab and/or inotuzumab
• Primary refractory disease (defined as failure to achieve a CR at the end of at least 1 induction chemotherapy)
• First relapse occurring within 12 months from first remission
• ECOG performance status that is either 0 or 1 at screening.

Exclusion Criteria:

• Allogeneic HCT within 12 weeks prior to screening.
• Presence of isolated extra-medullary disease, testicular involvement or bulky disease
• Patients with concomitant genetic syndromes associated with bone marrow failure states: such as patients with Fanconi anemia, Kostmann syndrome, Shwachman syndrome.
• Patients with Burkitt's lymphoma/leukemia
• History of active neurological auto immune or inflammatory disorders Other protocol-defined inclusion/exclusion criteria may apply.

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• Leukemia
• Leukemia, Lymphoid
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Drug:
• IMJ995 single agent
Single intravenous administration of IMJ995

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Novartis Pharmaceuticals

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence and nature of Dose Limiting Toxicities (Dose Escalation part only, in pediatric, adolescent and young adult ALL patients)	Dose recommendation for IMJ995 in pediatric, adolescent and young adult ALL patients	28 days
Primary	Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) (pediatric, adolescent and young adult ALL patients)	Safety and tolerability	24 months
Primary	Number of patients infused with planned target dose	Manufacture success rate	24 months
Secondary	Incidence and nature of DLTs during the first 28 days after IMJ995 infusion (safety cohort for adult ALL).	Dose recommendation in adult ALL	28 days
Secondary	Cellular kinetics of IMJ995 (maximum drug concentration - Cmax)	CAR transgene levels will be measured by flow cytometry and quantitative polymerase chain reaction (qPCR) in peripheral blood. PK parameters will be determined using non-compartmental methods for IMJ995.	24 months
Secondary	Cellular kinetics of IMJ995 (area under the drug concentration-time curve - AUC)	CAR transgene levels will be measured by flow cytometry and quantitative polymerase chain reaction (qPCR) in peripheral blood. PK parameters will be determined using non-compartmental methods for IMJ995.	24 months
Secondary	Number of participants with anti-CAR19 and/or anti-CAR22 antibodies	Humoral immunogenicity	24 months
Secondary	Change from baseline in interferon (IFN)-gamma levels in peripheral blood mononuclear cells (PBMCs)	Cellular immunogenicity	24 months
Secondary	Antitumor activity assessed by Complete Remission / Complete Remission with Incomplete Hematologic Recovery (CR/ CRi).	Antitumor activity	24 months
Secondary	Antitumor activity assessed by duration of response.	Duration of response	24 months
Secondary	Incidence and severity of AEs and SAEs after IMJ995 infusion (safety cohort for adult ALL).	Safety and tolerability	24 months