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Clinical Trials List

Protocol Number61186372PANSC2003
Active

2024-06-01 - 2026-12-31

Phase I

Not yet recruiting5

Recruiting1

ICD-10C34.90

Malignant neoplasm of unspecified part of unspecified bronchus or lung

ICD-10C34.91

Malignant neoplasm of unspecified part of right bronchus or lung

ICD-10C34.92

Malignant neoplasm of unspecified part of left bronchus or lung

ICD-10C7A.090

Malignant carcinoid tumor of the bronchus and lung

ICD-10Z51.12

Encounter for antineoplastic immunotherapy

ICD-9162.9

Malignant neoplasm of bronchus and lung, unspecified

A Phase 1/2 Open-label Platform Study to Evaluate the Safety and Efficacy of Multiple Amivantamab-based Therapeutic Combinations in Participants with Lung Cancer (LC)

  • Trial Applicant

    Johnson & Johnson

  • Sponsor

    Janssen Research & Development, LLC

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2026/02/01

Investigators and Locations

Principal Investigator TSUNG -YING YANG Division of Thoracic Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator 黃文聰 Division of Hematology & Oncology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator JIN-YUAN SHIH Division of General Internal Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator 林聖皓 Division of Thoracic Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator Jen-Yu Hung Division of Thoracic Medicine

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

The Actual Total Number of Participants Enrolled

0 Recruiting

Condition/Disease

Lung Cancer (LC)

Objectives

The primary objective of the Phase 1 Combination Dose Selection is to identify the recommended Phase 2 combination dose(s) (RP2CD[s]) of amivantamab-based combination therapies in participants with lung cancer. The primary objective of the Phase 2 Expansion is to evaluate the antitumor effect of amivantamab-based combination therapies, when administered at the selected RP2CD(s).

Test Drug

injection

Active Ingredient

amivantamab
DOCETAXEL

Dosage Form

270
270

Dosage

50 mg/ml
20 mg/ml

Endpoints

Incidence and severity of AEs, including DLTs

Inclution Criteria

Will be provided in each ISA

Exclusion Criteria

Will be provided in each ISA

The Estimated Number of Participants

  • Taiwan

    24 participants

  • Global

    100 participants