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NCT05541822 | RECRUITING | Advanced Solid Tumors

To Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetic Profile of ABN401 in Patients With Advanced Solid Tumors Harboring c-MET Dysregulation
Sponsor:

ABION INC

Brief Summary:

ABN401-003 is a Phase 2 clinical study to assess efficacy, safety, tolerability and pharmacokinetic profile of ABN401 in specific populations of advance solid tumors with c-MET alterations as monotherapy.

Condition or disease

Advanced Solid Tumors

Intervention/treatment

ABN401

Phase

PHASE2

Detailed Description:

This study will start with one cohort. Two additional cohorts are under consideration and the study will be a parallel cohort expansion study.

Study Type : INTERVENTIONAL
Estimated Enrollment : 40 participants
Masking : NONE
Primary Purpose : TREATMENT
Official Title : A Phase 2 Multicenter, Open-Label, Parallel Cohort Expansion Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetic Profile of ABN401 in Patients With Advanced Solid Tumors Harboring c-Mesenchymal-epithelial Transition Factor (c-MET) Dysregulation
Actual Study Start Date : 2023-01-17
Estimated Primary Completion Date : 2025-04
Estimated Study Completion Date : 2025-08

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • 1. Male or female ≥ 18 years of age or designated age of majority according to the regulatory authorities, whichever is higher.
  • 2. Eastern Cooperative Oncology Group (ECOG) performance status (PS), 0 or 1.
  • 3. Have a life expectancy of at least 3 months.
  • 4. Diagnosis
    • 1. must have histologically or cytologically confirmed NSCLC, advanced, recurrent, or metastatic,
    • 2. For Cohort 1: MET exon 14 skipping suspected by local or central biomarker assessment. \[local testing is accepted for eligibility; all patients will have confirmation by central laboratory, but this result is not necessary for eligibility; local molecular pathology result will suffice\]. This testing can be from archival or fresh tissue sample and/or blood specimen; any sample, any test positive subjects are eligible.
    • 5. Treatment experience
    • a. Cohort 1: Anti-tumor treatment naïve subject upon refusal to receive 1st line standard of care, or not tolerated to 1st line standard of care, or progressed after standard of care with no greater than 2 prior treatment regimens (neoadjuvant, adjuvant, and maintenance therapies do not qualify as separate treatment regimens).
    • 6. At least one measurable lesion per response evaluation criteria in solid tumors (RECIST) 1.1, with the exception of bone-only disease (i.e., non-measurable disease per RECIST 1.1) with at least 1 radiological non-target lesion.
    • 7. If not menopausal or surgically sterile, willing to practice at least one of the following highly effective methods of birth control for at least a (partner's) menstrual cycle before and for 3 months after study drug administration
      • 1. Barrier type devices (examples are condom, diaphragm, and contraceptive sponge) used only in combination with a spermicide
      • 2. Sexual intercourse with vasectomized male/sterilized female partner,
      • 3. Hormonal female contraceptive (oral, parenteral, intravaginal, implantable, or transdermal) for at least 3 consecutive months prior to investigational product administration (when not clinically contraindicated as in breast, ovarian and endometrial cancers),
      • 4. Use of an intrauterine contraceptive device. Note: Abstinence, the rhythm method, and/or contraception by the partner are not acceptable methods of birth control
      • 8. Resolution of prior-therapy-related AEs (including immune-related AEs but excluding alopecia) to ≤ Grade 1 per CTCAE v 5.0, and no treatment for these AEs for at least 2 weeks prior to the time of enrollment. Alopecia, sensory neuropathy Grade ≤ 2, or other Grade ≤ 2 AEs not constituting a safety risk based on investigator's judgment are acceptable.
      • 9. Adequate organ function as indicated by laboratory values.
      • 10. Tissue and blood specimens
      • 1. Willing to undergo a new biopsy or have available archival formalin-fixed, paraffin-embedded tumor tissue specimen. The archival tissue must be
        • * collected after progression from most recent prior systemic anti-cancer treatment, OR
        • * tissue samples collected prior to previous lines of treatment,
        • 2. ALL subjects must undergo blood sample for biomarker assessment.
        • 11. Able and willing to comply with the protocol and the restrictions and assessments therein.
        Exclusion Criteria
        • 1. Previous severe hypersensitivity reaction to any component of study drug(s).
        • 2. Prior therapy
        • a. Previous treatment with c-MET inhibitors or hepatocyte growth factor (HGF)-targeting therapy.
        • 3. Genetic analysis results
          • a. Cohort 1: Existing genetic data from the patient's tumor tissue showing known molecular alterations which would make them eligible for targeted therapies (e.g., EGFR mutations, ALK rearrangements, KRAS mutation, ROS1 translocation, BRAF mutation, RET alteration, and NTRK fusion, etc.).
          • 4. Chronic inflammatory liver condition. History or clinical evidence of any significant liver or biliary pathology including cirrhosis, infectious disease, inflammatory conditions, steatosis, or cholangitis (including ascending cholangitis, primary sclerosing cholangitis, obstruction, perforation, fistula of biliary tract, spasm of sphincter of Oddi, biliary cyst or biliary atresia).
          • 5. Presence or history of interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis
          • 6. Impairment of GI function or GI disease that may significantly alter the absorption of ABN401 (e.g., ulcerative diseases, uncontrolled nausea, uncontrolled vomiting, uncontrolled diarrhea, or malabsorption syndrome)
          • 7. Prior organ or stem cell transplant.
          • 8. Known active infection with human immunodeficiency virus (HIV), human T-cell leukemia virus, type (HTLV-1), hepatitis B virus (HBV), or hepatitis C virus (HCV), unless the patients fall into below categories (patients fall into one of the a, b, c category are eligible to participate)
          • a. HIV
          • * CD4+ cells ≥ 350 cells/µL
          • * No history of AIDS
          • * No history of opportunistic infection in the past 12 months b. HCV
          • * Undetectable viral load (Participants positive for hepatitis C antibody are eligible only if polymerase chain reaction is negative for hepatitis C RNA) c. HBV
          • * Concurrent HBV treatment and undetectable viral load (Participants with a past or resolved hepatitis B infection defined as the presence of hepatitis B core antibody \[anti-HBc\] and absence of hepatitis B surface antigen are eligible)
          • 9. Symptomatic ascites or pleural effusion, unless clinically stable for at least two weeks following treatment for these conditions (including therapeutic thoraco- or paracentesis).
          • 10. Known active central nervous system (CNS) primary tumor or metastases and/or carcinomatous meningitis. Patients with previously treated brain metastases may participate provided they are clinically stable for at least 4 weeks prior to first dose of ABN401, have no evidence of new or enlarging brain metastases and are off steroids for at least 15 days prior to first dose of ABN401.
          • 11. Presence or history of a malignant disease other than disease to be treated in current protocol that has been diagnosed and/or required therapy within the past 3 years. Exceptions to this exclusion include the following: completely resected basal cell and squamous cell skin cancers, indolent malignancies that currently do not require treatment, and completely resected carcinoma in situ of any type.
          • 12. Active infection requiring therapy. However, subject with minor infections requiring oral antibiotics, (e.g., urinary tract infection, Upper respiratory tract infection, etc.) could be eligible based on investigator's judgement.
          • 13. Use of systemic corticosteroids \> 10 mg/day prednisone or equivalent within 30 days or other immunosuppressive drugs within 30 days prior to first drug administration.
          • 14. Patients receiving treatment with medications that meet one of the following criteria and that cannot be discontinued at least 1 week prior to the start of treatment with ABN401 and for the duration of the study
          • * Strong and moderate inhibitors/inducers of P-glycoprotein
          • * Strong and moderate inhibitors/inducers of CYP3A4
          • * Proton pump inhibitors (PPI)
          • 15. Has received or will receive a live vaccine within 30 days prior to the first administration of study medication. Seasonal flu vaccine that does not contain live vaccine are permitted.
          • 16. Received an investigational product or treated with an investigational device within 30 days prior to first ABN401 administration.
          • 17. Has been receiving: radiotherapy, chemotherapy, or molecularly-targeted agents or tyrosine kinase inhibitors within 2 weeks (4 weeks in case of thoracic radiotherapy to lung fields) or 5 half-lives (whichever is longer) of the start of study treatment; immunotherapy/monoclonal antibodies within 3 weeks of the start of study treatment; nitrosoureas, antibody-drug conjugates, or radioactive isotopes within 6 weeks of the start of study treatment; 7-day washout is permitted for palliative radiation (i.e. limited field, ≤ 14-day course of radiotherapy) to non-CNS lesions.
          • 18. History or clinical evidence of any surgical or medical condition which the investigator judges as likely to interfere with the results of the study or pose an additional risk in participating e.g., rapidly progressive or uncontrolled disease involving a major organ system-vascular, cardiac, pulmonary, gastrointestinal, gynecologic, hematologic, neurologic, neoplastic, renal, endocrine, autoimmune or an immunodeficiency, or clinically significant active psychiatric or abuse disorders.
          • 19. Is a regular user (including "recreational use") of any illicit drugs or had a recent history (within the last year) of substance abuse (including alcohol).
          • 20. Pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the study.
          • 21. Patients with a corrected QT interval (using Fridericia's correction formula) (QTcF) of \> 470 msec (females) and \> 450 msec (males).
To Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetic Profile of ABN401 in Patients With Advanced Solid Tumors Harboring c-MET Dysregulation

Location Details

NCT05541822

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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

RECRUITING

United States, Florida

Cancer Care of North Florida, PA (Lake City Cancer Care, LLC) - Medical Oncology

Lake City, Florida, United States, 32024-3456

RECRUITING

United States, Florida

Mid Florida Center

Orange City, Florida, United States, 32763-8316

NOT YET RECRUITING

United States, Road cancer

The Henry Ford Cancer Institute

Detroit, Road cancer, United States, 48202

RECRUITING

United States, Texas

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States, 77030-4000

RECRUITING

Korea, Republic of, Gone

National Cancer Center

Shaky, Gyeongggi-do, Korea, Republic of, 10408

RECRUITING

Korea, Republic of, Ravy

University Hospital upgrade

Suwon, Gyeongggi-do, Korea, Republic of, 16499

RECRUITING

Korea, Republic of, Seoul

Boramae Medical Center

Shit, Seoul, Korea, Republic of, 07061

RECRUITING

Korea, Republic of, Seoul

Severance Hospital

Sinchon-dong, Seoul, Korea, Republic of, 03776

RECRUITING

Korea, Republic of,

Chungbuk National University Hospital

Cheongju-Si, Korea, Republic of, 28645

RECRUITING

Korea, Republic of,

Gachon University Gil Medical Center

Incheon, Korea, Republic of, 21565

RECRUITING

Korea, Republic of,

Gyeongsang National University Hospital

jin大发-公司, Korea, Republic of, 52728

RECRUITING

Korea, Republic of,

Seoul National University Bundang Hospital

Seongnam-shi, Korea, Republic of, 13620

RECRUITING

Korea, Republic of,

Korea University Anam Hospital

Seoul, Korea, Republic of, 02841

RECRUITING

Korea, Republic of,

hospital's Book of hospital

Seoul, Korea, Republic of, 03181

RECRUITING

Korea, Republic of,

Asan Medical Center

Seoul, Korea, Republic of, 05505

RECRUITING

Korea, Republic of,

Samsung Medical Center

Seoul, Korea, Republic of, 06351

RECRUITING

Korea, Republic of,

The Catholic University of Korea, Seoul St Mary's Hospitals

Seoul, Korea, Republic of, 06591

RECRUITING

Korea, Republic of,

The Catholic University of Korea St Vincents Hospital

Suwon, Korea, Republic of, 16248

RECRUITING

Taiwan,

China Medical University Hospital

Taichung, Taiwan, 404

RECRUITING

Taiwan,

CH IMEI hospital, l IO u shadow

Tainan City, Taiwan, 736

RECRUITING

Taiwan,

National Cheng If University Hospital

Tainan, Taiwan, 704

RECRUITING

Taiwan,

National Taiwan University Hospital

Taipei City, Taiwan, 100

RECRUITING

Taiwan,

National Taiwan University Cancer Center (NTUCC)

Taipei, Taiwan, 10052

RECRUITING

Taiwan,

Taipei Veterans General Hospital

Taipei, Taiwan, 112