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Phase 2 Completed N=17 Treatment

Study of CRS-207, Pembrolizumab, Ipilimumab, and Tadalafil in Metastatic Pancreatic Cancer

Source: ClinicalTrials.gov NCT05014776 ↗
Enrolled (actual)
17
Serious AEs
70.6%
Results posted
Jan 2025
Primary outcomePrimary: Objective Response Rate (ORR) Using Response Evaluation Criteria for Solid Tumors (RECIST 1.1) — 0 Participants

Summary

The purpose of this study is to evaluate the safety and clinical activity of tadalafil, pembrolizumab, ipilimumab, and CRS-207 in subjects with metastatic pancreatic adenocarcinoma who have progressed after at least 1 prior chemotherapy regimen.

Outcome Measures

OutcomeResultp-value
PRIMARY
Objective Response Rate (ORR) Using Response Evaluation Criteria for Solid Tumors (RECIST 1.1)
SECONDARY
Number of Participants Experiencing Drug-Related Adverse Events (AEs) Requiring Treatment Discontinuation

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years.
  • Have histologically or cytologically proven adenocarcinoma of the pancreas.
  • Have previously treated metastatic disease.
  • Have radiographic disease progression.
  • Patients with the presence of at least one measurable tumor lesion.
  • Patient's acceptance to have a tumor biopsy at baseline and on
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Patients must have adequate organ and marrow function defined by study-specified laboratory tests.
  • For both Women and Men, must use acceptable form of birth control while on study.
  • Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria

  • Known history or evidence of brain metastases.
  • Had chemotherapy, radiation, or biological cancer therapy within the last 14 days.
  • Have received an investigational agent or device within the last 28 days.
  • Had surgery within the last 28 days.
  • Expected to require any other form of systemic or localized cancer therapy while on study.
  • Have received a vaccine within the last 14 days (7 days for the COVID vaccine) or received a live vaccine within the last 30 days.
  • Have received steroids within the last 14 days.
  • Use more than 4 g/day of acetaminophen.
  • Use of organic nitrates.
  • Use of guanylate cyclase (GC) stimulators such as riociguat.
  • Consumption of substantial amounts of alcohol (≥5 units/day)
  • Use of strong or moderate cytochrome P450 3A4 (CYP3A4) inhibitor or inducer.
  • Patients on immunosuppressive agents within the last 7 days
  • Known allergy to both penicillin and sulfa.
  • Severe hypersensitivity reaction to any monoclonal antibody.
  • History of severe hypersensitivity to tadalafil.
  • Have implant(s) or device(s) that has not and cannot be easily removed.
  • Have artificial joints or implanted medical devices that cannot be easily removed.
  • Have any evidence of clinical or radiographic ascites.
  • Have significant and/or malignant pleural effusion
  • Uncontrolled intercurrent illness.
  • Subjects with active, known or suspected autoimmune disease.
  • Have a tissue or organ allograft, including corneal allograft.
  • Have been diagnosed HIV, Hepatitis B or C positive.
  • Is on supplemental home oxygen.
  • Has an unhealed surgical wound or ulcer, or a bone fracture considered non-healing.
  • Has clinically significant heart disease
  • Prior history of non-arterial ischemic optic retinopathy.
  • History of significant hypotensive episode requiring hospitalization within 6 months.
  • Has insufficient peripheral vein access.
  • Is unwilling or unable to follow the study schedule for any reason.
  • Is pregnant or breastfeeding.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05014776). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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