Combined AlloStim+Anti-PD-L1 in MSS Metastatic Colorectal Cancer

Phase 2

Not yet recruiting

• Conditions: Metastatic Colorectal Cancer

• Registration Number: NCT06557278
• Lead Sponsor: Mirror Biologics, Inc.

Brief Summary

Experimental immunotherapy in chemotherapy-refractory and immunotherapy-refractory metastatic colorectal cancer patients that have progressed, or are intolerant to, Longsurf (TAS-102) +/- Avastin (bevacizumab) or Stivarga (regorafenib) combining experimental AlloStim with an anti-programmed death ligand 1 (PD-L1) checkpoint inhibitor drug.

Detailed Description

The protocol provides fourth-line experimental treatment for subjects with microsatellite stable (MSS)/ proficient mismatch repair (pMMR) metastatic colorectal cancer. These patients do not respond to checkpoint inhibitors. This study will investigate whether AlloStim® administered weekly in three-21 day cycles with each cycle consisting of 3 weekly intradermal (ID) doses followed the last week with an intravenous (IV) dose (3 cycles =Days 0 through 77) can prime patients to become responsive to checkpoint inhibition immunotherapy. A restaging computed tomography (CT) scan is conducted on day 84 after the priming and will be compared to the baseline CT scan by Response Evaluation Criteria in Solid Tumors (RECIST 1.1). Scans at day 84 are expected to be read as radiological progression upon restaging after AlloStim® priming possibly due to immunological swelling, known as "pseudoprogression", consistent with the presumed inflammatory mechanism of action of AlloStim®. This mechanism may convert "cold" tumors to "hot" tumors. The immune cell infiltrates of tumors after AlloStim® include T-helper cell type 1 (Th1) memory cells which produce interferon-gamma. Interferon-gamma is known to increase expression of anti-programmed death ligand 1 (PD-L1) checkpoint molecules in the tumor microenvironment. Higher PD-L1 expression may convert checkpoint inhibitor unresponsive tumors to become checkpoint inhibitor responsive. After three 21-day cycles of AlloStim® priming, a combination of AlloStim® IV boosters and anti-PD-L1 checkpoint therapy (with avelumab 800 mg q/2 weeks) is scheduled between days 91 to day161, A restaging CT scan at day 175 is then compared to day 84 and baseline to determine if the tumor target lesions' size has changed.

Study Timeline

• Status Verified: 2024-08
• Study First Submitted: 2024-08-08
• Study First Submitted QC: 2024-08-13
• Last Update Submitted: 2024-08-13
• Study First Posted: 2024-08-16
• Last Update Posted: 2024-08-16
• Study Start: 2024-09
• Primary Completion: 2025-12
• Study Completion: 2026-03

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Adult male and female subjects aged 18-80 years at screening visit

2. Pathologically confirmed diagnosis of MSS/pMMR colorectal adenocarcinoma

3. Presenting with metastatic disease:

   • Primary tumor can be intact or previously resected

4. Previous treatment failure of at least two lines of active systemic chemotherapy:

   • Previous chemotherapy must have included a fluoropyrimidine, oxaliplatin (e.g. FOLFOX, CAPOX), and irinotecan-containing (e.g. FOLFIRI) regimens (single regimen of FOLFIRINOX satisfies)
   • Administered in adjuvant setting or for treatment of metastatic disease
   • If KRAS wild type, must have at least one prior anti-EGFR therapy if left sided primary tumor

5. Treatment failure or refusal/not qualified for at least one third-line treatment

   • TAS-102 +/- bevacizumab or regorafenib
   • Treatment failure can be due to disease progression or toxicity
   • Time from last treatment failure to Informed Consent must be no more than 30 days

6. ECOG performance score: 0-1

7. Adequate hematological function:

   • Absolute granulocyte count ≥ 1,200/mm3
   • Platelet count ≥ 100,000/mm3
   • Hemoglobin ≥ 9.0 g/dL (may be corrected by transfusion)

8. Adequate Organ Function:

   • Creatinine ≤ 1.5 mg/dL
   • Total bilirubin ≤ 1.5 times upper limit of normal (ULN)

9. Alkaline phosphatase ≤ 2.5 times ULN *

10. Aspartate aminotransferase (AST) or (SGOT) ≤ 2.5 times ULN *

11. Alanine aminotransferase (ALT) or (SGPT) ≤ 2.5 times ULN*

12. EKG without clinically relevant abnormalities

13. Female subjects: Not pregnant or lactating

14. Patients with childbearing potential must have a negative ß-HCG test and agree to use a highly effective contraceptive method during the course of the study

15. Study specific Informed Consent in the native language of the subject

    • ≤ 5 times ULN if liver involvement

Exclusion Criteria

1. High frequency microsatellite instability (MSI-H) or deficient mismatched repair dMMR

2. Bowel obstruction or high risk for obstruction if tumors become inflamed

3. Moderate or severe ascites requiring medical intervention

4. Clinical evidence of brain metastasis or leptomeningeal involvement

5. Widespread peritoneal carcinomatous (e.g. CT scan shows innumerable lesions visible and/or abnormal thickening of greater omentum) that increases risk of a major morbidity (e.g. bowel obstruction) in the opinion of the Investigator

6. COPD

7. Pulmonary lymphangitis or symptomatic pleural effusion (grade ≥ 2) that results in pulmonary dysfunction requiring active treatment; or, oxygen saturation <92% on room air

8. Any of the following mood disorders: active major depressive episode, recent history of suicidal attempt or ideation

9. Prior allogeneic bone marrow/stem cell or solid organ transplant

10. Chronic use (> 2 weeks) of greater than physiologic doses of a corticosteroid agent (dose equivalent to > 5 mg/day of prednisone) planned or anticipated during the study before the end of the Safety Evaluation Period (28 days after the last dose of IP)

    • Topical corticosteroids are permitted

11. Prior diagnosis of an active autoimmune disease (e.g., rheumatoid arthritis, multiple sclerosis, autoimmune thyroid disease, uveitis)

    • Well controlled Type I diabetes allowed (HbA1c < 8.5%)

12. Prior experimental immunotherapy

13. History of blood transfusion reactions

14. Progressive viral or bacterial infection

    o All infections must be resolved and the subject must remain afebrile for seven days without antibiotics prior to being placed on study

15. Cardiac disease of symptomatic nature

16. History of HIV positivity or AIDS

17. History of severe hypersensitivity to monoclonal antibody drugs

18. Psychiatric or addictive disorders or other condition that, in the opinion of the Investigator, would preclude study participation.

19. Subjects that lack ability to provide consent for themselves

20. Any prior cancer diagnosis (other than cured basal cell carcinoma, head and neck carcinoma in-situ, superficial Ta, Tis, T1 bladder cancer, or papillary carcinoma of thyroid) or concurrent cancer histologically different than colorectal adenocarcinoma

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Objective Tumor Response	day 168	CT scan RESIST 1.1
Overall Survival	2 years	survival from signing consent until death by any cause

Trial Locations

Locations (3)

New York Cancer and Blood Specialists; 🇺🇸 Shirley, New York, United States

Mt. Sinai Comprehensive Cancer Center; 🇺🇸 Miami Beach, Florida, United States

Hirschfield Oncology Center; 🇺🇸 Brooklyn, New York, United States