Clinical trial · Interventional
Grapiprant (ARY-007) and Pembrolizumab in Patients With Advanced or Metastatic Post-PD-1/L1 NSCLC Adenocarcinoma
Open Label, Single Arm, Phase 1b/2 Study to Evaluate the Safety and Efficacy of Grapiprant (ARY-007) in Combination With Pembrolizumab in Patients With Advanced or Metastatic Post-PD-1/L1 Non-Small Cell Lung Cancer (NSCLC) Adenocarcinoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Based on the totality of the generated combined safety and efficacy data in the interim period, the company decided to terminate the combination study in NSCLC patients. There are no subjects on study drug at this time or in the EOT Follow-up period.
Summary
Brief summary (as posted)
This study will be conducted in adult participants diagnosed with NSCLC who have been previously treated for a minimum of 12 weeks with any PD-1 or PD-L1 checkpoint inhibitor. This is a phase 1b/2, multi-center, open label study designed to assess safety and tolerability of grapiprant in combination with pembrolizumab, to determine the recommended phase 2 dose (RP2D) with pembrolizumab, and to evaluate disease response with grapiprant based on investigator assessments. Pharmacokinetics, pharmacodynamics and response biomarkers will also be assessed.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-small Cell Lung Cancer Adenocarcinoma | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| grapiprant and pembrolizumab | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- grapiprant and pembrolizumab combination
- description
- Participants will be treated with grapiprant in combination with pembrolizumab.
- interventionNames
- Drug: grapiprant and pembrolizumab
Primary outcomes (3)
- measure
- Safety and tolerability of grapiprant in combination with pembrolizumab
- timeFrame
- Up to 90 days after the end of treatment (average of 7 months)
- description
- Number of incidence, severity, relationship, concomitant medications administered, and duration of treatment emergent adverse events using CTCAE v5.0
- measure
- Define the recommended phase 2 dose (RP2D) of grapiprant combined with pembrolizumab
- timeFrame
- Through Cycle 1 (21 days)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Key Inclusion Criteria: * Male and female adult patients at least 18 years of age on day of signing informed consent * Histologically confirmed non-small cell lung cancer (NSCLC) adenocarcinoma * Advanced (stage IIIb) disease that is not amenable to curative intent treatment with concurrent chemoradiation and metastatic (stage IV) patients * Progressed clinically and/or radiographically per RECIST v1.1 after receiving a PD-1 or PD-L1 antagonist for a minimum of 12 weeks * Measurable disease per RECIST v1.1 * Disease that can be safely accessed via bronchoscopic, thoracoscopic or percutaneous biopsy for multiple core biopsies and participant is willing to provide tissue from newly obtain biopsies on study in a subgroup of patients * Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 * Adequate organ function * Highly effective birth control * Able to swallow and absorb oral tablets Key Exclusion Criteria: * Current use of NSAIDs, COX-2 inhibitors * Known epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), ROS gene alteration * No history of smoking (≤100 cigarettes lifetime) * History of severe hypersensitivity reactions to a PD-1/L1 antibody * Received prior systemic anti-cancer therapy including investigational agents within 4 weeks prior to treatment or 5 half-lives, whichever is shorter * Received prior radiotherapy within 2 weeks of start of study treatment * Has received a live vaccine within 30 days prior to the first dose of study treatment * Taking strong CYP3A4 or P-glycoprotein inhibitors or inducers * Diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior the first dose of study treatment * Known additional malignancy that is progressing or has required active treatment within the past 3 years (with some permitted exceptions) * Known active CNS metastases and/or carcinomatous meningitis * Active autoimmune disease that has required systemic treatment in past 2 years * History of pneumonitis that required steroids or has current pneumonitis * Has an active infection requiring systemic therapy * Recent or current GI ulcer, colitis or non-immune colitis * Known history of human immunodeficiency virus (HIV) infection, or known active Hepatitis B, or Hepatitis C virus infection * Has had an allogeneic tissue/solid organ transplant * Clinically significant (i.e.active) cardiovascular disease
References
Publications (0)
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