Status:
COMPLETED
Keynatinib in Treated Patients With NSCLC and Brain Metastases
Lead Sponsor:
Medolution Ltd.
Conditions:
Non-Small Cell Lung Cancer With EGFR Mutation
Brain Metastases
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to evaluate the safety and efficacy of Keynatinib capsules in patients with advanced non-small cell lung cancer (NSCLC) with brain metastasis or progression of brain metas...
Detailed Description
This is a multicenter, non-randomized, open, single-arm, phase IIa trial investigating the security and effectiveness of Keynatinib in patients with advanced non-small cell lung cancer (NSCLC) with br...
Eligibility Criteria
Inclusion
- Unlimited gender, age ≥ 18 years；
- Histologically or cytologically documented locally advanced, metastatic NSCLC (including L858R and/or Exon19 del mutation positive). The EGFR mutation assessed by local laboratory/or central laboratory via tissue/cytology or in plasma;
- Subjects should have the following conditions: a. (Cohort 1) Progression on any of the first or second generation EGFR inhibitors (gefitinib, erlotinib, afatinib, etc.).B. (Cohort 2) Progression on any third generation EGFR inhibitor (oxitinib, etc.), prior or non-prior treatment with any first or second generation EGFR inhibitor;
- The peripheral lesions did not progress after EGFR inhibitor treatment, but the occurrence of brain metastasis or progression of brain metastasis was confirmed by magnetic resonance imaging (MRI);
- As determined by the investigator, no final surgical resection or radiotherapy is expected for all lesions;
- Stable condition for at least 2 weeks prior to study medication without any corticosteroid or anticonvulsant therapy;
- The status score of Eastern Cooperative Oncology Group (ECOG) is 0 to 1 points, and there was no deterioration during the first 2 weeks of enrollment;
- Estimated survival time \> 3 months；
- Sufficient bone marrow, liver, kidney and blood coagulation function；
- Subjects must be willing to use barrier contraception；
- Ability to provide informed consent, complete all study assessments and have complete medical record.
Exclusion
- Have previously received chemotherapy, immunotherapy or any other systemic antitumor therapies within 4 weeks before the first administration; Have previously received EGFR-TKI within 5× half-life before the first administration; Have received oral fluorouracil and other small-molecule targeted drugs (whichever is longer) within 2 weeks or 5× half-life before enrollment; Within 2 weeks before enrollment, subjects had received palliative radiotherapy for non-target lesions for symptom relief, and traditional Chinese medicine (including Chinese patent medicine) for tumor indication;
- Have received whole brain radiation therapy;
- Only leptomeningeal metastasis are present;
- Historical intracranial hemorrhage not related to the tumor;
- Major organ surgery (excluding needle biopsy) or significant trauma have been performed within 4 weeks prior to enrollment;
- The drug or food with strong inhibition or induction of cytochrome P450 (CYP) isoenzyme CYP3A4 could not be stopped. The drug or food with strong inhibition or induction of cytochrome P450 (CYP) isoenzyme CYP3A4 had been used within 7 days before enrollment;
- Any unresolved toxicities from prior therapy greater than CTCAE 5.0 grade 1 at the time of enrollment with the exception of alopecia;
- Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the tablet or previous significant bowel resection that would preclude adequate absorption of Keynatinib;
- Past medical history of ILD, drug-induced ILD, radiation pneumonitis which required steroid treatment, or CT scan at baseline revealed the presence of idiopathic pulmonary fibrosis; Uncontrolled large pleural effusion or pericardial effusion; Active tuberculosis;
- Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension and active bleeding diatheses or active infection including hepatitis B, hepatitis C and HIV;
- Have a history of severe cardiovascular disease (NYHA cardiac function grade III or IV);
- Other primary malignancies (except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix) within 5 years;
- Allergic to the active ingredient or excipient of Keynatinib;
- Pregnant or lactating women.
Key Trial Info
Start Date :
October 21 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 10 2024
Estimated Enrollment :
16 Patients enrolled
Trial Details
Trial ID
NCT04824079
Start Date
October 21 2020
End Date
December 10 2024
Last Update
January 22 2025
Active Locations (5)
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1
Cancer Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China, 100021
2
Fujian Cancer Hospital
Fuzhou, Fujian, China, 350014
3
Henan Cancer Hospital
Zhengzhou, Henan, China, 450003
4
Hunan Cancer Hospital
Changsha, Hunan, China, 410013