ACTolog in Patients With Solid Cancers

Cancer Clinical Trial

— ACTolog  

Official title:

Phase I Adoptive Cellular Therapy Trial With Endogenous CD8+ T Cells (ACTolog® IMA101) Alone or in Combination With Atezolizumab in Patients With Relapsed and/or Refractory Solid Cancers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02876510
• Other study ID #: IMA101-101
• Status: Completed
• Phase: Phase 1
• Start date: June 30, 2017
• Est. completion date: September 22, 2021

Study information

• Verified date: February 2024
• Source: Immatics US, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study purpose is to learn about the safety and tolerability of IMA101 alone (Cohort 1) or in combination with atezolizumab (Cohort 2) in patients with advanced solid cancers that express pre-defined Immatics tumor targets.

Description:

SCREENING: Patient eligibility will be determined by HLA (human leukocyte antigen) and the main biomarkers screening. If the patient is eligible, white blood cells will be collected with a leukapheresis for the manufacture of the IMA101 product.

MANUFACTURE: IMA101 product will be made from the patient's white blood cells.

TREATMENT: IMA101 product will be administered to the patient intravenously after lymphodepleting pre-conditioning with chemotherapy (fludarabine and cyclophosphamide).

Low-dose IL-2 will be self-administered twice daily for a total of 28 doses after infusion of IMA101 product. In Cohort 2, atezolizumab will be administered every 3 weeks, starting no earlier than 3 weeks after the IMA101 product infusion and after hematologic recovery.

Patients will be monitored closely throughout the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: September 22, 2021
• Est. primary completion date: September 22, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Patients must have pathologically confirmed advanced/metastatic cancer prior to enrollment.

2. HLA phenotype positive.

3. Eastern Cooperative Oncology Group (ECOG) performance status 0-1.

4. Life expectancy > 6 months prior to enrollment.

5. Patient is a candidate for a maximum of one further line of established therapy (prior to treatment with ACTolog).

6. The patient has adequate organ and marrow function per protocol

7. At least one lesion (metastasis or primary tumor) being considered accessible by non-high-risk collection procedures for biopsy.

8. The patient has adequate hepatic function per protocol

9. The patient has serum creatinine clearance =50 mL/min by the Cockcroft-Gault formula.

10. The patient has adequate pulmonary function per protocol

11. Acceptable coagulation status

12. Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation.

13. Male subjects must agree to use effective contraception or abstinence while on study and for 90 days after infusion of the ACTolog T-cell product.

14. Ability of subject to understand and the willingness to sign written informed consent for study participation.

15. Confirmed availability of production capacities for the patient's ACTolog products.

16. ACTolog target expression as evaluated by the in vitro diagnostic device IMA_Detect:

Patient's tumor must express at least one ACTolog target as assessed by quantitative PCR (qPCR) (to be assessed from a tumor biopsy to be performed if all other eligibility criteria are met).

Exclusion Criteria

1. Any condition contraindicating leukapheresis.

2. Patients with brain metastases. Patients with a history of brain metastases may be eligible, if an imaging scan with contrast enhancement not older than 4 weeks is able to exclude the existence of currently active brain metastasis.

3. HIV infection, active Hepatitis B or C infection, or active infections requiring oral or intravenous antibiotics or that can cause a severe disease and pose a severe danger to lab personnel working on patients' blood or tissue. If positive test results are not indicative of an active infection, patients can be included.

4. Treatment with excluded therapy per protocol

5. Previous extensive radiotherapy to the lung or liver during the last 4 months prior to lymphodepletion regimen.

6. The patient has cardiac conditions defined per protocol

7. Patients with prior stem cell transplantation or solid organ transplantation.

8. The patient has concurrent severe and/or uncontrolled medical disease that could compromise participation in the study

9. Active diverticulitis, intra-abdominal abscess, gastrointestinal obstruction, abdominal carcinomatosis or other known risk factors for bowel perforation.

10. History of other malignancies (except for adequately treated basal or squamous cell carcinoma or carcinoma in situ) within the last 3 years.

11. The patient is pregnant or is breastfeeding.

12. Serious autoimmune disease per protocol

13. History of hypersensitivity to cyclophosphamide, fludarabine or IL-2.

14. Immunosuppression, not related to prior treatment for malignancy.

15. History of or current immunodeficiency disease or prior treatment compromising immune function at the discretion of the treating physician.

16. Patients with Grade 3 or higher immune-related toxicities related to prior checkpoint inhibitors

Related Conditions & MeSH terms

• Cancer
• Solid Tumor

Intervention

Drug:
• Fludarabine
Fludarabine infusion
• Cyclophosphamide
Cyclophosphamide infusion

Biological:
• IMA101 product
i.v. infusion of IMA101 product(s).
• Recombinant human interleukin-2
Low dose IL-2 Infusion for two weeks

Diagnostic Test:
• IMADetect
IMADetect is a laboratory test that is part of screening used to determine the mRNA expression of ACTolog target source genes in tumor biopsies from solid tumors. IMADetect is intended for investigational use only.

Drug:
• Atezolizumab
Atezolizumab infusion will be given no earlier than 3 weeks post IMA101 infusion and after hematologic recovery is achieved, thereafter every 3 weeks until 1 year after IMA101 infusion.

Locations

Country	Name	City	State
United States	University of Texas MD Anderson Cancer Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Immatics US, Inc.	M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of adverse events (Safety and tolerability) of IMA101 alone or in combination with atezolizumab		up to 18 months
Secondary	Peripheral T-cell persistence (assessment of frequency of T-cells over time)		up to 18 months
Secondary	Tumor response per Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 and immune-related RECIST (irRECIST)		up to 18 months