ORIC-114 in Combination With Subcutaneous Amivantamab in Patients With EGFR Exon20 Insertion Mutant NSCLC

Официальное название

Phase 1b Study of ORIC-114 in Combination With Amivantamab in Patients With EGFR Exon20 Insertion Mutant NSCLC

Обзор

The purpose of this study is to establish the recommended phase 2 dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of ORIC-114 in combination with subcutaneous (SC) amivantamab in patients with advanced or metastatic NSCLC harboring an EGFR exon 20 insertion mutation.

Подробное описание

ORIC-114, is a brain penetrant, selective, orally bioavailable, irreversible small molecule inhibitor designed to target EGFR exon 20 insertion mutations, making it a promising therapeutic candidate for development in patients whose tumors harbor these alterations, including those with CNS metastases.

Amivantamab is a bispecific EGFR-directed and MET receptor-directed antibody indicated in combination with carboplatin and pemetrexed for the first line treatment of patients with locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations and also as a single agent in patients with locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations whose disease has progressed on or after platinum-based chemotherapy.

This is an open-label, single arm, multicenter, dose escalation followed by dose expansion study to assess the safety and preliminary antitumor activity of ORIC-114 in combination with SC amivantamab, in patients with locally advanced or metastatic NSCLC harboring an EGFR exon 20 insertion mutations.

Вмешательства

• Препарат ORIC-114 Dose 1 + amivantamab
  ORIC-114 oral daily, amivantamab subcutaneous weekly for 4 weeks followed by every 4 week injection
• Препарат ORIC-114 Dose 2 + amivantamab
  ORIC-114 oral daily, amivantamab subcutaneous weekly for 4 weeks followed by every 4 week injection
• Препарат ORIC-114 Dose 3 + amivantamab
  ORIC-114 oral daily, amivantamab subcutaneous weekly for 4 weeks followed by every 4 week injection

Первичные конечные точки

• Recommended Phase 2 Dose (RP2D) [Срок оценки: 12 months]
• Objective response rate (ORR) [Срок оценки: 12 months]
• Duration of response (DOR) [Срок оценки: 12 months]
• Progression-free survival (PFS) [Срок оценки: 12 months]

Вторичные конечные точки (9)

• Plasma PK parameters [Срок оценки: 28 Days]
• Plasma PK parameters [Срок оценки: 28 Days]
• Plasma PK parameters [Срок оценки: 28 Days]
• Plasma PK parameters [Срок оценки: 28 Days]
• BICR-Objective response rate (ORR) [Срок оценки: 12 months]
• BICR-Duration of response (DOR) [Срок оценки: 12 months]
• BICR-Progression-free survival (PFS) [Срок оценки: 12 months]
• Intracranial Objective response rate (ORR) [Срок оценки: 12 months]
• Intracranial Progression-free survival (PFS) [Срок оценки: 12 months]

Критерии участия

Критерии включения

• Histologically or cytologically confirmed metastatic NSCLC with a documented EGFR exon 20 insertion mutation as determined locally by any nucleic acid-based diagnostic testing method; all tests should be performed in a CLIA certified or equivalently accredited laboratory
• Prior Therapies:

• Dose Escalation: Patients may have previously received and progressed on or after platinum-based chemotherapy or may be treatment naïve
• Dose Expansion: Patients must not have received any prior therapy; at time of enrollment, patients must decline, or be ineligible for all available standard of care therapies with proven benefit
• Agreement and ability to undergo a pretreatment biopsy, provided the procedure is clinically feasible and not deemed unsafe by the investigator
• Measurable disease according to RECIST 1.1
• Patients with asymptomatic CNS metastases are eligible
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Adequate organ function

Критерии исключения

• Known small cell lung cancer transformation
• Leptomeningeal disease
• Spinal cord compression not definitively treated with surgery or radiation
• Prior immunotherapy
• Past medical history of interstitial lung disease (ILD), drug induced ILD, radiation pneumonitis which required steroid treatment, or any evidence of clinically active ILD
• Active gastrointestinal disease (eg, Crohn's disease, ulcerative colitis, or short gut syndrome) or other malabsorption syndromes that would reasonably impact absorption of ORIC-114

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Нерандомизированное

Модель

Последовательный дизайн

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

США · 2 центра

• NYU Langone Health — New York
• Virginia Cancer Specialists — Fairfax

Австралия · 1 центр

• Peter MacCallum Cancer Centre — Melbourne

Канада · 1 центр

• The Princess Margaret Hospital — Toronto

Идентификаторы

NCT: NCT06816992 · ORIC-114-05

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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