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OncoMatch/Clinical Trials/NCT07774520

A Randomized Study to Evaluate the Efficacy of a Reduced Starting Dose of Lazertinib (Leclaza) and Preemtive Magnesium Supplementation to Prevent Lazertinib(Leclaza)-Induced Peripheral Neuropathy

Is NCT07774520 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies multiple treatments including Supplementation of magnesium lactate and Dose reduction of lezertinib for non-small cell lung cancer(nsclc).

Phase 2RecruitingSamsung Medical CenterNCT07774520Data as of Sep 2026Location: South Korea

Treatment: Supplementation of magnesium lactate · Dose reduction of lezertinibLazertinib is currently approved as a first-line treatment for EGFR-mutant NSCLC in South Korea. However, many patients experience peripheral neuropathy, which causes severe numbness, tingling, or painful muscle cramps. This side effect significantly lowers patients' quality of life and often leads to treatment interruptions. This phase 2, open-label, randomized clinical trial newly diagnosed EGFR mutant NSCLC patients is based on the hypothesis that a lower dose of lazertinib combined with magnesium supplementation will result in a more tolerable safety profile without compromising efficacy outcomes

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Dose reduction of lezertinib

Other

Supplementation of magnesium lactate

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: EGFR exon 19 deletion

Required: EGFR l858r

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≥ 19

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07774520 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require EGFR?

Yes, EGFR exon 19 deletion is a required biomarker for enrollment.

Does this trial require EGFR?

Yes, EGFR l858r is a required biomarker for enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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