For Healthcare Professionals

TAK-788 as First-Line Treatment Versus Platinum-Based Chemotherapy for Non-Small Cell Lung Cancer (NSCLC) With EGFR Exon 20 Insertion Mutations

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About the study

The purpose of this study is to compare the effectiveness of TAK-788 as first-line treatment with that of platinum-based chemotherapy in participants with locally advanced or metastatic non-small cell lung cancer (NSCLC) whose tumors has epidermal growth factor receptor (EGFR) exon 20 insertion mutations. Participants will be randomly assigned to one of the two treatment groups- TAK-788 group or Platinum-based chemotherapy group. Participants will receive TAK-788 orally and pemetrexed/cisplatin or pemetrexed/carboplatin via vein until the participants experience worsening disease (PD) as assessed by blinded independent review committee (IRC), intolerable harmful effects or another discontinuation criteria.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

  1. Male or female adult patients (aged 18 years or older)
  2. Histologically or cytologically confirmed nonsquamous cell locally advanced not suitable for definitive therapy, recurrent, or metastatic (Stage IV) NSCLC
  3. Documented epidermal growth factor receptor (EGFR) in-frame exon 20 insertion mutation assessed by a clinical laboratory improvements amendment (CLIA)-certified (US sites) or an accredited (outside of the US) local laboratory The EGFR exon 20 insertion mutation can be either alone or in combination with other EGFR or human epidermal growth factor receptor 2 (HER2) mutations except EGFR mutations for which there are approved anti-EGFR tyrosine kinase inhibitors [TKIs] (ie, exon 19 del, L858R, T790M, L861Q, G719X, or S768I, where X is any other amino acid)
  4. Adequate tumor tissue available, either from primary or metastatic sites, for central laboratory confirmation of EGFR exon 20 insertion mutation
  5. At least 1 measurable lesion per RECIST Version 1.1
  6. Life expectancy ≥3 months
  7. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
  8. Adequate organ and hematologic function as defined by blood transfusions with a recommended >/ 14 day washout period.

EXCLUSION CRITERIA

  1. Received prior systemic treatment for locally advanced or metastatic disease, including local administration, such as intra-pleural injection of anticancer medication with the exception noted below:
  2. Neoadjuvant or adjuvant chemotherapy/immune therapy for Stage I to III or combined modality chemotherapy/radiation for locally advanced disease is allowed if completed >6 months before the development of metastatic disease.
  3. Received radiotherapy ≤14 days before randomization or has not recovered from radiotherapy-related toxicities
  4. Received a moderate or strong cytochrome P450 (CYP)3A inhibitor or moderate or strong CYP3A inducer within 10 days before first dose of TAK-788
  5. Have been diagnosed with another primary malignancy other than NSCLC
  6. Have current spinal cord compression or leptomeningeal disease
  7. Have uncontrolled hypertension. Participants with hypertension should be under treatment on study entry to control blood pressure
  8. Received a live vaccine within 4 weeks before randomization per Summary of product characteristics (SmPCs) for pemetrexed, cisplatin, and carboplatin
  9. Taking medication(s) known to be associated with the development of torsades de pointes.
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
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Study’s details


Contition

Advanced/Metastatic Non-Small Cell Lung Cancer (NSCLC)

Age

18+

Phase

Phase 3

Participants needed

354

Est. Completion Date

Jun 2026

Treatment type

Interventional


Sponsor

Takeda

ClinicalTrials.gov identifier

NCT04129502

Study number

TAK-788-3001

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