Olaptesed With Pembrolizumab and Nanoliposomal Irinotecan or Gemcitabine/Nab-Paclitaxel in MSS Pancreatic Cancer

Official title

An Open-label Phase 2 Study of Olaptesed Pegol (NOX-A12) Combined With Pembrolizumab and Nanoliposomal Irinotecan/5-FU/Leucovorin or Gemcitabine/Nab-paclitaxel in Microsatellite-stable Metastatic Pancreatic Cancer Patients

Overview

The purpose of this study is to provide a go/no-go decision for a randomized expansion study by assessing the disease control rate (DCR) at 6 weeks for the combination of olaptesed pegol on top of pembrolizumab and (Arm 1) nanoliposomal irinotecan, 5-FU and leucovorin or (Arm 2) gemcitabine and nab-paclitaxel, to assess safety and tolerability and time-to-event endpoints.

Interventions

• Drug Olaptesed pegol
  400 mg per week as continous infusion until progression or intolerable toxicity
• Drug Pembrolizumab
  200 mg every 3 weeks as i.v. infusion until progression or intolerable toxicity or a maximum of 35 administrations

Primary outcome measures

• Go/no-go decision for a randomized expansion study [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]

Secondary outcome measures (8)

• Safety and tolerability [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• DCR at 12 weeks [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• Progression free survival (PFS) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• Overall response rate (ORR) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• median Overall survival (mOS) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• Duration of response (DOR) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• Time-to-best overall response (TBOR) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]
• Time-to-next-anticancer-treatment (TTNT) [Time frame: until progression or intolerable toxicity to completion of 35 administrations (approximately 2 years) with pembrolizumab]

Eligibility criteria

Inclusion criteria

• Patient with confirmed microsatellite-stable tumor pathology, if data available
• Patient with histologically or cytologically confirmed primary metastatic adenocarcinoma of the pancreas, who

• Arm 1: stopped first-line treatment with gemcitabine/nab-paclitaxel after documented objective radiographic progression OR
• Arm 2: stopped first-line treatment with FOLFIRINOX or modified FOLFIRINOX after documented objective radiographic progression
• Measurable disease based on RECIST 1.1 as determined by the investigational site
• Estimated minimum life expectancy 3 months
• Eastern Cooperative Oncology Group (ECOG) performance score 0 to 1
• Adequate organ function laboratory values within the ranges specified: Serum albumin ≥ 3.0 g/dL; Hematological system: Hemoglobin (Hb) ≥ 9.0 g/dL or ≥5.6 mmol/L, Absolute neutrophil count (ANC) ≥ 1,500/mm³, Platelets ≥ 100,000/mm³; Renal system: Creatinine ≤ 1.5 x ULN OR eGFR ≥30 mL/min for patient with creatinine levels >1.5 × institutional ULN; Hepatic system: Total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ULN for patients with total bilirubin levels >1.5 × ULN, ALT and AST ≤ 2.5 x ULN (≤5 × ULN for patients with liver metastases); Coagulation: INR OR PT ≤ 1.5 x ULN unless patient is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants, aPTT ≤ 1.5 x ULN unless patient is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants

Exclusion criteria

• Prior systemic anti-cancer therapy including investigational agents within 4 weeks or 5 half-lives, whichever is shorter, prior to treatment.
• Patients must have recovered from all AEs due to previous therapies to ≤ Grade 1 or baseline. Patients with ≤ Grade 2 neuropathy may be eligible. Patients with endocrine-related AEs Grade ≤2 requiring treatment or hormone replacement may be eligible.
• If the patient had major surgery, the patient must have recovered adequately from the procedure and/or any complications from the surgery prior to starting study intervention
• Prior radiotherapy within 2 weeks of start of study treatment. Patients must have recovered from all radiation-related toxicities, not require corticosteroids, and not have had radiation pneumonitis.
• Prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX 40, CD137) and discontinued from that treatment due to a Grade 3 or higher irAE
• Diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior the first dose of study drug
• Received a live or live-attenuated vaccine within 30 days prior to the first dose of study intervention. Administration of killed vaccines are allowed
• Active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
• History of (non-infectious) pneumonitis / interstitial lung disease that required steroids or current pneumonitis / interstitial lung disease
• Active infection requiring systemic therapy
• Known additional malignancy that is progressing or has required active treatment within the past 2 years.
• Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
• Pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 120 days after the last dose of study treatment
• Previous allogeneic tissue/solid organ transplant

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Parallel assignment

Masking

Single blind

Primary purpose

Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT04901741 · SNOXA12C701 · 2021-001963-25 · KEYNOTE-B01 · MK-3475-B01

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗