Combination of amivantamab and tepotinib for treating MET-altered non-small cell lung cancer

An Open-Label Phase I/II Study to Evaluate the Safety and prelimiBasnary Efficacy of Amivantamab and Tepotinib Combination in MET-altered Non-small Cell Lung Cancer (NSCLC)

This study is testing a combination of two drugs, amivantamab and tepotinib, to see if they can help people with a specific type of lung cancer called MET-altered non-small cell lung cancer.

Quick facts

• Phase: Phase1; Phase2
• Study type: Interventional
• Enrollment: 60 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: M.D. Anderson Cancer Center (Academic / other)
• Drugs / interventions: amivantamab, tepotinib, capmatinib, savolitinib, crizotinib, osimertinib, chemotherapy, immunotherapy, radiation, prednisone, amivantmab
• Locations: 1 site (Houston, Texas)
• Trial ID: NCT06083857 on ClinicalTrials.gov

What this trial studies

This clinical trial aims to evaluate the safety and efficacy of the drug combination amivantamab and tepotinib in patients with MET-altered non-small cell lung cancer (NSCLC). The study consists of a safety run-in phase to determine the recommended dose and an efficacy phase to assess the objective response rate in different patient cohorts. Participants will undergo genomic profiling to explore potential resistance mechanisms and clinical benefits associated with the treatment. The trial will also monitor the safety and tolerability of the drug combination throughout the study.

Who should consider this trial

Good fit: Ideal candidates for this study are adults aged 18 and older with advanced MET-altered non-small cell lung cancer that is not amenable to curative surgery or radiotherapy.

Not a fit: Patients with non-MET-altered NSCLC or those who have already received treatment with amivantamab or tepotinib may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with MET-altered NSCLC, potentially improving their response rates and overall outcomes.

How similar studies have performed: Other studies have shown promising results with similar targeted therapies in MET-altered NSCLC, indicating potential for success with this combination approach.

Eligibility criteria

Inclusion Criteria:

1. Written informed consent and HIPAA authorization for release of personal health inf ormation prior to registration. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
2. Age ≥ 18 years at the time of consent.
3. Histologically or cytologically confirmed non-small cell lung cancer.
4. Locally advanced or metastatic disease, not amenable to curative surgery or radiotherapy.
5. Patients must have one of the following:

   * NSCLC which harbors MET Exon 14 skipping alterations detected in the tissue or ctDNA (safety cohort and cohort A \[MET ex14 TKI-naïve\] and B \[MET ex14 TKI-refractory\])
   * MET gene amplification determined in tissue by next-generation sequencing (NGS) as copy-number gain (CNG\>=10) or FISH assay (MET:CEP7\>=2.0) (safety cohort and cohort C \[MET amplification or overexpression cohort\]
   * MET gene amplification determined in ctDNA (definition of gain per ctDNA testing platform) (safety cohort and cohort C \[MET amplification or overexpression cohort\]
   * MET overexpression by IHC 3+ (safety cohort and cohort C \[MET amplification or overexpression cohort\]
6. Eastern Cooperative Oncology Group (ECOG) performance status 0-1
7. Measurable disease per RECIST 1.1.
8. Patients with brain metastases are eligible if they are asymptomatic, are treated, or are neurologically stable for at least two weeks without the use of steroids or on stable or decreasing dose of ≤ 15 mg daily prednisone (or equivalent).
9. Ability to take pills by mouth.
10. Previous treatment with cytotoxic chemotherapy or immunotherapy is allowed.
11. Patients must have adequate bone marrow and organ functions.

    * Hemoglobin ≥10 g/dL
    * ANC ≥1.5 x 109 /L
    * Platelets ≥75 x 10 9 /L
    * AST and ALT ≤3 x ULN
    * Total bilirubin ≤1.5 x ULN; subjects with Gilbert's syndrome can enroll if conjugated bilirubin is within normal limits
    * Serum creatinine \<1.5 x ULN or if available, calculated or measured creatinine clearance \>50 mL/min/1.73 m2 ALT = alanine aminotransferase; ANC = absolute neutrophil count; AST = aspartate aminotransferase; ULN = upper limit of normal
12. A woman of childbearing potential must have a negative serum pregnancy test at screening and within 7 days of the first dose of study treatment and must agree to further serum or urine pregnancy tests during the study.
13. A woman must be compliant with the Contraceptive Guidance and Collection of Pregnancy Information:

    1. Not of childbearing potential
    2. Of child-bearing potential and practicing true abstinence during the entire period of the study, including up to 6 months after the last dose of study treatment is given
    3. Of childbearing potential and practicing 2 methods of contraception, including 1 highly effective user independent method and a second method.

    Participant must agree to continue contraception throughout the study and through 6 months after the last dose of study treatment.

    • Note: If the childbearing potential changes after start of the study (eg, woman who is not heterosexually active becomes active, premenarchal woman experiences menarche) the woman must begin birth control, as described above.
14. A woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the study and for 6 months after receiving the last dose of study treatment.
15. A man must wear a condom when engaging in any activity that allows for passage of ejaculate to another person during the study and for 6 months after receiving the last dose of study treatment. A man who is sexually active with a woman of childbearing potential must agree to use a condom with spermicidal foam/gel/film/cream/suppository and his partner must also be practicing a highly effective method of contraception (ie, established use of oral, injected, or implanted hormonal methods of contraception; placement of an intrauterine device \[IUD\] or intrauterine hormone-releasing system \[IUS\]).

    If the participant is vasectomized, he must still use a condom (with or without spermicide) for prevention of passage of exposure through ejaculation, but his female partner is not required to use contraception.
16. A male participant must agree not to donate sperm for the purpose of reproduction during the study and for a minimum of 6 months after receiving the last dose of study treatment.
17. Participant must be willing and able to adhere to the lifestyle restrictions specified in this protocol.

Exclusion Criteria:

1. For cohort A (METex14 TKI-naïve only), prior targeted therapy to c-MET is not allowed, which includes small molecule TKIs, such as tepotinib, capmatinib, savolitinib, or crizotinib. Prior amivantamab is also not allowed.
2. Patients whose tumor harbors other oncogene-driver mutations, such as EGFR mutation, KRASG12C mutation, ALK-fusion, with prior targeted therapies, such as osimertinib, sotorasib, and other TKI, are not allowed.
3. Positive hepatitis B (hepatitis B virus \[HBV\]) surface antigen (HBsAg) Note: Subjects with a prior history of HBV demonstrated by positive hepatitis B core antibody are eligible if they have at Screening 1) a negative HBsAg and 2) a HBV DNA (viral load) below the lower limit of quantification, per local testing. Subjects with a positive HBsAg due to recent vaccination are eligible if HBV DNA (viral load) is below the lower limit of quantification, per local testing.
4. Positive hepatitis C antibody (anti-HCV). Note: Subjects with a prior history of HCV, who have completed antiviral treatment and have subsequently documented HCV RNA below the lower limit of quantification per local testing are eligible.
5. Other clinically active or chronic liver disease.
6. Participant is positive for human immunodeficiency virus (HIV), with 1 or more of the following:

   * Receiving ART that may interfere with study treatment (consult with Principal Investigator for review of medication prior to enrollment)
   * CD4 count \<350 at screening
   * AIDS-defining opportunistic infection within 6 months of start of screening
   * Not agreeing to start ART and be on ART\>4 weeks plus having HIV viral load \<400 copies/mL at end of 4-week period (to ensure ART is tolerated and HIV controlled).
7. Participant has active cardiovascular disease including, but not limited to:

   * A medical history of deep vein thrombosis or pulmonary embolism within 1 month prior to first dose of study drug or any of the following within 6 months prior to the first dose of study drug: myocardial infarction, unstable angina, stroke, transient ischemic attack, coronary/peripheral artery bypass graft, uncontrolled hypertension, clinically significant cardiac arrythmia, or any acute coronary syndrome. Clinically non-significant thrombosis, such as non-obstructive catheter-associated clots, incidental or asymptomatic pulmonary embolism, are not exclusionary.
   * Congestive heart failure (CHF), defined as New York Heart Association (NYHA) class III-IV or hospitalization for CHF (any NYHA class; refer to Appendix: New York Heart Association Criteria) within 6 months of study Day 1.
8. Subject has uncontrolled inter-current illness, including but not limited to poorly controlled diabetes, ongoing or active infection (i.e., has discontinued all antibiotics for at least one week prior to first dose of study drug), or psychiatric illness/social situation that would limit compliance with study requirements. Subjects with medical conditions requiring chronic continuous oxygen therapy are excluded.
9. Any ophthalmologic condition that is clinically unstable (consult with Principal Investigator for review of the condition prior to enrollment).
10. Participant has an active or past medical history of ILD/pneumonitis, including drug-induced or radiation ILD/pneumonitis.
11. Immune-mediated rash from prior treatment that has not resolved prior to enrollment.
12. Any unresolved toxicities from prior therapy greater than CTCAE grade 1 (with the exception of alopecia grade 2) at the time of starting study treatment.
13. Participant has concurrent or prior malignancy other than the disease under study. The following exceptions require consultation with the Medical Monitor:

    1. Non-muscle invasive bladder cancer (NMIBC) treated within the last 24 months that is considered completely cured. b. Skin cancer (non-melanoma or melanoma) treated within the last 24 months that is considered completely cured. c. Non-invasive cervical cancer treated within the last 24 months that is considered completely cured.

Where this trial is running

Houston, Texas

• MD Anderson Cancer Center — Houston, Texas, United States (Recruiting)

Study contacts

• Principal investigator: Xiuning Le, MD,PHD — M.D. Anderson Cancer Center
• Study coordinator: Xiuning Le, MD,PHD

Conditions Non-small Cell Lung Cancer