CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 776 enrolled / 776 target
Drug / intervention
Lazertinib +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04988295
NCT04988295Phase 3ActiveUpdate Overdue (14.0/mo)Completion was 35mo ago

A Phase 3, Open-Label, Randomized Study of Amivantamab and Lazertinib in Combination With Platinum-Based Chemotherapy Compared With Platinum-Based Chemotherapy in Patients With EGFR-Mutated Locally Advanced or Metastatic Non-Small Cell Lung Cancer After Osimertinib Failure

Janssen Research & Development, LLC·interventional·Posted Aug 3, 2021·Updated Jun 8, 2026

In Brief

A Phase 3 clinical trial evaluating Lazertinib, Amivantamab, and 2 other interventions for Carcinoma, Non-Small-Cell Lung. Active but no longer recruiting, targeting 776 participants across 249 sites in 29 countries.

Signals

Enrollment appears stalled

Detailed Summary

The purpose of this study is to assess the efficacy of adding lazertinib to amivantamab, carboplatin, and pemetrexed (LACP/ACP-L dosing strategies) and amivantamab, carboplatin and pemetrexed (ACP) compared with carboplatin and pemetrexed (CP) in participants with locally advanced or metastatic epidermal growth factor receptor (EGFR) Exon 19del or Exon 21 L858R substitution non-small cell lung cancer (NSCLC) after osimertinib failure. The purpose of the extension cohort is to further describe the safety and efficacy for the ACP-L dosing schedule versus ACP with additional data. After completion of the primary analysis, the study may eventually transition to an open-label extension (OLE) or long-term extension (LTE) phase during which participants will have the option to continue their assigned treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesArgentina, Belgium, Brazil, Bulgaria, Canada, China, Czechia, Denmark, France, Germany, Hong Kong, India, Israel, Italy, Japan, Malaysia, Mexico, Netherlands, Poland, Portugal, Puerto Rico, Russia, South Korea, Spain, Sweden, Taiwan, Turkey (Türkiye), United Kingdom, United States
Collaborators--

Timeline

Phase 3Active
2022202320242025202620272028
First PostedAug 3, 2021
Enrollment StartNov 17, 2021
Primary CompletionJul 10, 2023
Study CompletionNov 30, 2027
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 4.9 years ago

Arms & Interventions

Arm A: LACP/ACP-Lexperimental

LACP dosing (study start until 6 November 2022): Participants will receive Lazertinib orally along with Amivantamab, Pemetrexed, and Carboplatin as IV infusion starting on Cycle 1 Day 1 for 4 cycles (each cycle consists of 21 days). After 4 cycles, participants will receive Amivantamab, Pemetrexed and Lazertinib as maintenance until disease progression. ACP-L dosing (from 7 November 2022 until study completion): Participants will receive Amivantamab, Pemetrexed, and Carboplatin starting on Cycle 1 Day 1 for 4 cycles. Lazertinib in ACP-L will start on Cycle 5 Day 1 or sooner if carboplatin is discontinued before cycle 4 (each cycle consists of 21 days). Beginning with Cycle 5 Day 1, participants will receive Amivantamab, Pemetrexed and Lazertinib as maintenance until disease progression.

Drug: LazertinibDrug: AmivantamabDrug: PemetrexedDrug: Carboplatin
Arm B: CP (Carboplatin and Pemetrexed)active_comparator

Participants will receive Pemetrexed in combination with Carboplatin as IV infusion for up to 4 cycles (each cycle consists of 21 days). After 4 cycles, participants will receive Pemetrexed as maintenance until disease progression.

Drug: PemetrexedDrug: Carboplatin
Arm C: ACP (Amivantamab, Carboplatin and Pemetrexed)experimental

Participants will receive Amivantamab, Pemetrexed, and Carboplatin as IV infusion for up to 4 cycles (each cycle consists of 21 days). After 4 cycles, participants will receive Amivantamab and Pemetrexed as maintenance until disease progression.

Drug: AmivantamabDrug: PemetrexedDrug: Carboplatin
Arm A2 (Extension Cohort): ACP-Lexperimental

Participants will receive Amivantamab, Pemetrexed and Carboplatin as IV infusion for up to 4 cycles (each cycle consists of 21 days), Lazertinib will start on C5D1 or sooner if carboplatin is discontinued earlier). After 4 cycles, participants will receive Pemetrexed, Amivantamab, Lazertinib as maintenance until disease progression.

Drug: LazertinibDrug: AmivantamabDrug: PemetrexedDrug: Carboplatin
Arm C2 (Extension Cohort): ACPexperimental

Participants will receive Amivantamab, Pemetrexed, and Carboplatin as IV infusion for up to 4 cycles (each cycle consists of 21 days). After 4 cycles, participants will receive Amivantamab and Pemetrexed as maintenance until disease progression.

Drug: AmivantamabDrug: PemetrexedDrug: Carboplatin

Interventions

Lazertinibdrug

Lazertinib will be administered orally.

Amivantamabdrug

Amivantamab will be administered as an IV infusion.

Pemetrexeddrug

Pemetrexed will be administered as an IV infusion.

Carboplatindrug

Carboplatin will be administered as an IV infusion.