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Clinical Trials/NCT06772623
NCT06772623
Recruiting
Phase 1

An Open-label Multi-Cohort Phase 1b/2 Study to Evaluate the Safety, Efficacy, and Optimal Dose of Telisotuzumab Adizutecan in Combination With a PD-1 Immune Checkpoint Inhibitor in Advanced or Metastatic Non-Squamous NSCLC With No Prior Treatment for Advanced Disease and No Actionable Genomic Alterations

AbbVie101 sites in 9 countries252 target enrollmentMarch 6, 2025

Overview

Phase
Phase 1
Intervention
Telisotuzumab Adizutecan
Conditions
Non Small Cell Lung Carcinoma
Sponsor
AbbVie
Enrollment
252
Locations
101
Primary Endpoint
Part 1: Dose-Limiting Toxicities (DLT)s of Telisotuzumab Adizutecan
Status
Recruiting
Last Updated
2 months ago

Overview

Brief Summary

Non small cell lung carcinoma (NSCLC) is the most frequently occurring histologic subtype of lung cancer and is the leading cause of cancer-related deaths worldwide. The purpose of this study is to assess adverse events and change in disease activity when Telisotuzumab Adizutecan (ABBV-400) is given in combination with a programmed cell death receptor 1 (PD1) immune checkpoint inhibitor to adult participants to treat NSCLC.

Telisotuzumab Adizutecan (ABBV-400) and budigalimab are investigational drugs being developed for the treatment of NSCLC. This study will be divided into two stages, with the first stage treating participants with several doses of telisotuzumab adizutecan in combination with budigalimab within the dose escalation regimen until the dose reached is tolerable and expected to be efficacious. In Stage 2 there will be 3 treatment groups. Two groups will receive pembrolizumab with different optimized doses of telisotuzumab adizutecan (to allow for the best dose to be studied in the future). One group will receive the standard of care (SOC) - pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed. Approximately 252 adult participants with NSCLC will be enrolled in the study in 132 sites worldwide.

In the dose escalation stage participants will be treated with increasing intravenous (IV) doses of Telisotuzumab Adizutecan in combination with budigalimab until the dose of Telisotuzumab Adizutecan reached is tolerable and expected to be efficacious. In the dose optimization stage participants will be receive IV optimized doses of Telisotuzumab Adizutecan in combination with IV pembrolizumab, or IV SOC - pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed. The study will run for a duration of approximately 33 months.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at an approved institution (hospital or clinic). The effect of the treatment will be frequently checked by medical assessments, blood tests, questionnaires and side effects.

Registry
clinicaltrials.gov
Start Date
March 6, 2025
End Date
November 1, 2027
Last Updated
2 months ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
AbbVie
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Must have histologically documented non-squamous (NSq) non small cell lung carcinoma (NSCLC) that is locally advanced or metastatic will be enrolled into the study.
  • Must have measurable disease per response evaluation criteria in solid tumors (RECIST) v1.
  • For Part 1, participants must have had no more than 1 systemic therapy for advanced disease including platinum-based chemotherapy or an immune checkpoint inhibitor (as monotherapy or in combination with chemotherapy), or appropriate targeted therapy for an actionable gene alteration, if applicable, for epidermal growth factor receptor (EGFR) wild-type (WT) NSq NSCLC.
  • For Part 2, participants must have no prior systemic therapy for advanced disease, no known actionable genomic alteration.
  • Must have documented programmed death ligand 1 (PD-L1) status.
  • For Part 2, participant must have evaluable c-Met immunohistochemistry (IHC) result per central testing prior to randomization.
  • Must have adequate organ function.

Exclusion Criteria

  • Known uncontrolled metastases to the central nervous system.
  • History of interstitial lung disease (ILD) or pneumonitis that required treatment with systemic steroids, or any evidence of active ILD or pneumonitis on screening chest computed tomography (CT) scan.

Arms & Interventions

Part 1: Telisotuzumab Adizutecan + Budigalimab

Participants will receive several doses of telisotuzumab adizutecan in combination with budigalimab, as part of the 33 month study duration.

Intervention: Telisotuzumab Adizutecan

Part 1: Telisotuzumab Adizutecan + Budigalimab

Participants will receive several doses of telisotuzumab adizutecan in combination with budigalimab, as part of the 33 month study duration.

Intervention: Budigalimab

Part 2 Arm 1: Telisotuzumab Adizutecan + Pembrolizumab

Participants will receive telisotuzumab adizutecan dose A in combination with pembrolizumab, as part of the 33 month study duration.

Intervention: Telisotuzumab Adizutecan

Part 2 Arm 1: Telisotuzumab Adizutecan + Pembrolizumab

Participants will receive telisotuzumab adizutecan dose A in combination with pembrolizumab, as part of the 33 month study duration.

Intervention: Pembrolizumab

Part 2 Arm 2: Telisotuzumab Adizutecan + Pembrolizumab

Participants will receive telisotuzumab adizutecan dose B in combination with pembrolizumab, as part of the 33 month study duration.

Intervention: Telisotuzumab Adizutecan

Part 2 Arm 2: Telisotuzumab Adizutecan + Pembrolizumab

Participants will receive telisotuzumab adizutecan dose B in combination with pembrolizumab, as part of the 33 month study duration.

Intervention: Pembrolizumab

Part 2: Standard of Care

Participants will receive pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed, as part of the 33 month study duration.

Intervention: Pembrolizumab

Part 2: Standard of Care

Participants will receive pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed, as part of the 33 month study duration.

Intervention: Carboplatin

Part 2: Standard of Care

Participants will receive pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed, as part of the 33 month study duration.

Intervention: Pemetrexed

Part 2: Standard of Care

Participants will receive pembrolizumab, pemetrexed, and investigator's choice of carboplatin or cisplatin, followed by pembrolizumab and pemetrexed, as part of the 33 month study duration.

Intervention: Cisplatin

Outcomes

Primary Outcomes

Part 1: Dose-Limiting Toxicities (DLT)s of Telisotuzumab Adizutecan

Time Frame: Up to Approximately 84 Days

DLT events are defined as clinically significant adverse events or abnormal laboratory values assessed as unrelated to disease progression, underlying disease, intercurrent illness, or concomitant medications.

Part 2: Objective Response (OR) as Assessed by Blinded Independent Central Review (BICR)

Time Frame: Up to Approximately 33 Months

OR is defined as confirmed complete response (CR) or confirmed partial response (PR) per BICR based on Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.

Number of Participants with Adverse Events (AE)s

Time Frame: Up to Approximately 33 Months

An adverse event is defined as any untoward medical occurrence in a participant or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment.

Secondary Outcomes

  • Part 1 and Part 2: PFS as Assessed by Investigator(Up to Approximately 33 Months)
  • Part 1 and Part 2: DOR as Assessed by Investigator(Up to Approximately 33 Months)
  • Part 1 and Part 2: DC as Assessed by Investigator(Up to Approximately 33 Months)
  • Part 1 and Part 2: Overall Survival (OS)(Up to Approximately 33 Months)
  • Programmed Death Ligand 1 (PD-L1) and c-Met Subgroups: OR(Up to Approximately 33 Months)
  • PD-L1 and c-Met Subgroups: PFS(Up to Approximately 33 Months)
  • PD-L1 and c-Met Subgroups: OS(Up to Approximately 33 Months)
  • PD-L1 and c-Met Subgroups: DOR(Up to Approximately 33 Months)
  • PD-L1 and c-Met Subgroups: DC(Up to Approximately 33 Months)

Study Sites (101)

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