MC# 21-38 - Multicenter, Randomized, Parallel Group, Phase II Study to Establish the Efficacy and Safety of Combinations of CBP501, Cisplatin, and Nivolumab for ≥3rd Line Treatment of Patients with Exocrine Pancreatic Cancer and WBC

  • Agent(s): CBP501
  • Disease Type(s): Pancreatic
  • Phase(s): II
  • Drug Classification(s): Targeted Therapy
  • Molecular Target(s): G2 Checkpoint

Mechanism of Action

CBP501, a G2 checkpoint inhibitor, inhibits multiple serine/threonine kinases, including MAPKAP-K2, C-Tak1, and CHK1, that phosphorylate serine 216 of the dual-specific phosphatase Cdc25C (cell division checkpoint 25 C); disruption of Cdc25C activity results in the inhibition of Cdc25C dephosphorylation of the mitotic cyclin-dependent kinase complex Cdc2/cyclin B, preventing entry into the mitotic phase of the cell cycle.

Purpose

In this study, the sponsor and investigators want to learn:

  • If CBP501 in combination with Cisplatin and/or Nivolumab shows any effect on reducing tumor growth
  • How much of CBP501 can be given in combination with Cisplatin and/or Nivolumab with an acceptable level of side effects
  • The effects of CBP501 (good and bad) when given in different combinations with Cisplatin and/or Nivolumab
Inclusion Criteria
  1. Signed informed consent obtained prior to initiation of any study-specific procedures and treatment
  2. Patients with pathologically confirmed stage IV exocrine pancreatic cancer who have received at least two lines of systemic therapy for metastatic disease.  Up to 10 of prior lines of systemic therapy (including prior cisplatin), chemoradiotherapy, radiotherapy or investigational agents the patient has received are allowed in order to be eligible, as long as all eligibility criteria are met, with the exception that a patient must not have received more than two prior lines incorporating anti-PD-1, anti-PD-L1, or anti-CTLA-4 immune checkpoint blockade.  Patients who have received prior anti-PD-1, anti-PD-L1, or anti-CTLA-4 immune checkpoint blockade therapy must have tolerated therapy with no evidence of grade 4 toxicity or an immune-related event (any grade) that required treatment discontinuation.  Patients who experienced an endocrine related dysfunction are eligible, provided they are on stable hormone replacement therapy.
  3. Male or female patients aged ≥ 18 years at time of informed consent
  4. ECOG Performance Status (PS) 0-1
  5. Life expectancy > 3 months
  6. Previous anticancer treatment must be discontinued at least 3 weeks prior to the initiation of study treatment (with the exception of 6 weeks for mitomycin C; 6 weeks for anti-androgen therapy if discontinued prior to treatment initiation, and 8 weeks for bicalutamide)
  7. Adequate bone marrow reserve, cardiac, liver, renal and metabolic function:
    • white blood cell count (WBC) <10,000/mm3;
    • absolute neutrophil count (ANC) ≥ 1,500/mm3;
    • platelet count ≥ 100,000/mm3;
    • hemoglobin ≥ 9 g/dL;
    • creatinine phosphokinase isozymes CPK-MB and CPK-MM;
    • serum troponin T levels within normal limits;
    • bilirubin ≤ 1.5 x ULN;
    • alanine aminotransferase (ALT, SGPT) and aspartate aminotransferase (AST, SGOT) ≤ 2.5 x ULN (≤ 5 x ULN if liver metastases are present);
    • INR ≤ 1.5 x ULN;
    • serum creatinine ≤ ULN or creatinine clearance ≥ 60 mL/min (by Cockcroft & Gault formula or alternate calculation by 24hr urine collection).  Patients with serum creatinine ≤ ULN and clearance between 45 to 59 mL/min should reduce cisplatin dose by 50%;
    • serum potassium ≥ 3.0 and ≤ 5.5 mmol/L;
    • serum calcium ≥ 8.0 and ≤ 11.5 mg/dL (≥ 2.0 and ≤ 2.9 mmol/L);
    • serum magnesium ≥ 1.2 and ≤ 3.0 mg/dL (≥ 0.5 and ≤ 1.23 mmol/L);
  8. Female patients of child-bearing potential must have a negative serum pregnancy test and use at least one form of contraception as approved by the investigator for 4 weeks prior to initiating study treatment and for 14 months after the last dose of study drug.  For the purposes of this study, child-bearing potential is defined as "all female patients unless they are post-menopausal for at least 3 years or surgically sterile.
  9. Male patients must use a form of barrier contraception approved by the investigator during the study and for 14 months after the last dose of study drug
  10. Ability to cooperate with study treatment and follow-up
Exclusion Criteria
  1. Radiation therapy to >30% of bone marrow prior to study entry
  2. Prior chemotherapy with nitrosoureas, prior mitomycin C cumulative dose ≥ 25 mg/m2, prior bone marrow transplant, or prior intensive chemotherapy with stem cell support
  3. Presence of any serious concomitant systemic disorders incompatible with the study in the opinion of the investigator (e.g., uncontrolled congestive heart failure, active infection, etc.)
  4. Any previous history of another malignancy (other than cured basal cell or squamous cell carcinoma of the skin or cured in-situ carcinoma) within 5 years of study entry
  5. Presence of any significant central nervous system (CNS) or psychiatric disorder(s) that would hamper the patient's compliance
  6. Evidence of peripheral neuropathy grade ≥ 2
  7. Treatment with any other investigational agent or participation in another clinical trial within 28 days prior to study entry
  8. Pregnant or breast-feeding patients or any patient with child-bearing potential not using adequate contraception
  9. Known HIV, HBV, or HCV infection (excluding cured HBV and/or cured HCV infection)
  10. Active CNS metastases; however, patients with CNS metastases will be eligible if they have been treated and are stable without symptoms for 4 weeks after completion of treatment, with image documentation required, and must be off steroids
  11. Who require chronic systemic steroid therapy or on any other form of immunosuppressive medication
  12. Has received a live-virus vaccination within 30 days of planned treatment start
  13. With known risk factors for bowel perforation, i.e., history of diverticulitis, intra-abdominal abscess, intestinal obstruction, or abdominal carcinomatosis
  14. Has an active autoimmune disease or a documented history of autoimmune disease
  15. Has a history pneumonitis or interstitial lung disease
  16. Patients who were permanently discontinued from prior immunotherapy due to immune-related adverse events
     

Location

  • Dallas, TX - Mary Crowley Cancer Research - Medical City
More Info: https://clinicaltrials.gov/ct2/show/NCT04953962

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Re: MC# 21-38