- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT06911008
MTI-301 do leczenia przerzutowych lub nieoperacyjnych i opornych na raka stałych
Badanie fazy I SCD I: Pierwsze w badaniu ustalania schematu dawki ludzkiej w celu oceny bezpieczeństwa, tolerancji, farmakokinetyki i aktywności MTI-301 u pacjentów z zaawansowaną nowotworami nowotworowymi
This phase I trial tests the safety, side effects, and best dose of MTI-301 in treating patients with solid cancers that have spread from where they first started (primary site) to other places in the body (metastatic) or that cannot be removed by surgery (unresectable) and that have not responded to previous treatment (refractory). MTI-301 is a drug that inhibits an enzyme called SCD1. SCD1 is an enzyme that promotes tumor growth and spread and is upregulated in some cancer types. MTI-301 may disrupt the activity of SCD1, which may lead to reduced tumor growth and/or spread.
Przegląd badań
Status
Warunki
Szczegółowy opis
PRIMARY OBJECTIVE:
I. To assess and determine the maximum tolerated dose (MTD) for SCD1 inhibitor MTI-301 (MTI-301).
SECONDARY OBJECTIVES:
I. To determine the toxicity profile with MTI-301. II. To determine objective response rate (ORR), progression free survival (PFS) and duration of response (DOR).
CORRELATIVE RESEARCH:
I. To characterize the pharmacokinetic (PK) profile of MTI-301. II. To assess the levels of SCD1 substrates steric acid, palmitic acid and products oleic acid, palmitoleic acid at baseline, at progression, and at the end of study.
III. To assess immune regulator factors from blood at baseline, at progression, and at the end of study.
OUTLINE: This is a dose-escalation study of MTI-301.
Patients receive MTI-301 orally (PO) once daily (QD) on days 1-28 of each cycle. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo computed tomography (CT), positron emission tomography (PET)/CT, or magnetic resonance imaging (MRI) and collection of blood samples throughout the study, and undergo tissue sample collection at baseline and at disease progression.
After completion of study treatment, patients are followed up every 3 months for up to 1 year.
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 1
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Clinical Trials Referral Office
- Numer telefonu: 855-776-0015
- E-mail: mayocliniccancerstudies@mayo.edu
Kopia zapasowa kontaktu do badania
- Nazwa: Cancer Center Clinical Trials
- Numer telefonu: 507-293-6386
Lokalizacje studiów
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Florida
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Jacksonville, Florida, Stany Zjednoczone, 32224-9980
- Rekrutacyjny
- Mayo Clinic in Florida
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Kontakt:
- Clinical Trials Referral Office
- Numer telefonu: 855-776-0015
- E-mail: mayocliniccancerstudies@mayo.edu
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Główny śledczy:
- Winston Tan, MD
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Kontakt:
- Cancer Center Clinical Trials
- Numer telefonu: 507-293-6386
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
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Age ≥ 18 years.
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Histologically or cytologically confirmed solid tumor (cancer) that is metastatic or unresectable and who are refractory to or intolerant of existing, standard-of-care therapy(ies), known to provide clinical benefit for their condition.
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Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) criteria or evaluable disease.
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Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2.
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Hemoglobin ≥ 9.0 g/dL (obtained ≤ 28 days prior to registration).
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Absolute neutrophil count (ANC) ≥ 1500/mm^3 (obtained ≤ 28 days prior to registration).
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Platelet count ≥ 100,000/mm^3 (obtained ≤ 28 days prior to registration).
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Total bilirubin ≤ 1.5 x upper limit normal (ULN). Patients with Gilbert's syndrome: Total bilirubin ≤ 3 x ULN (obtained ≤ 28 days prior to registration).
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Alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 3 x ULN (≤ 5 x ULN for patients with liver involvement) (obtained ≤ 28 days prior to registration).
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Prothrombin time (PT)/international normalized ratio (INR)/activated partial thromboplastin time (aPTT) =< 1.5 x ULN OR if patient is receiving anticoagulant therapy and INR or aPTT is within target range of therapy as determined by treating investigator (obtained ≤ 28 days prior to registration).
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Calculated creatinine clearance ≥ 60 mL/min using the Cockcroft-Gault formula (obtained ≤ 28 days prior to registration).
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Negative pregnancy test done ≤ 7 days prior to registration, for persons of childbearing potential only.
- NOTE: If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
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Provide written informed consent.
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Ability to complete questionnaire(s) by themselves or with assistance.
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Willingness to provide mandatory blood specimens for correlative research.
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Willingness to provide mandatory tissue specimens for correlative research.
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Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase of the study).
Exclusion Criteria:
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Any of the following because this study involves an investigational agent whose genotoxic, mutagenic, and teratogenic effects on the developing fetus and newborn are unknown:
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Pregnant persons
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Nursing persons
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Persons who are of childbearing potential who are unwilling to employ adequate contraception.
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NOTE: For the purpose of this guidance, methods that can achieve a failure rate of less than 1% per year when used consistently and correctly are considered as highly effective birth control methods. Such methods include:
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Combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation [Hormonal contraception may be susceptible to interaction with the investigational medicinal product (IMP), which may reduce the efficacy of the contraception method.]:
- Oral
- Intravaginal
- Transdermal
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Progestogen-only hormonal contraception associated with inhibition of ovulation (Hormonal contraception may be susceptible to interaction with the IMP, which may reduce the efficacy of the contraception method.):
- Oral
- Injectable
- Implantable (Contraception methods that in the context of this guidance are considered to have low user dependency.)
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Intrauterine device (IUD) (Contraception methods that in the context of this guidance are considered to have low user dependency)
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Intrauterine hormone-releasing system (IUS) (Contraception methods that in the context of this guidance are considered to have low user dependency.)
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Bilateral tubal occlusion (Contraception methods that in the context of this guidance are considered to have low user dependency.)
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Vasectomised partner [Contraception methods that in the context of this guidance are considered to have low user dependency. Vasectomised partner is a highly effective birth control method provided that partner is the sole sexual partner of the women of childbearing potential (WOCBP) trial participant and that the vasectomised partner has received medical assessment of the surgical success.]
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Sexual abstinence (In the context of this guidance sexual abstinence is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the subject.).
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Any of the following prior therapies:
- Major surgery ≤ 3 weeks prior to registration
- Chemotherapy ≤ 2 weeks prior to registration
- Immunotherapy ≤ 3 weeks prior to registration
- Radiation ≤ 2 weeks prior to registration.
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Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens.
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Immunocompromised patients and patients known to be HIV positive and currently receiving antiretroviral therapy, patients with hepatitis B and C on active treatment, or those with acute hepatitis B and C not currently on treatment.
- NOTE: Patients known to be HIV positive, but without clinical evidence of an immunocompromised state, are eligible for this trial.
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Uncontrolled intercurrent illness including, but not limited to:
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Clinically significant cardiac arrhythmia
- Bleeding disorder
- Cardiac arrhythmia
- Psychiatric illness/social situations that would limit compliance with study requirements
- Dyspnea at rest due to complications of advanced malignancy or other disease that requires continuous oxygen therapy
- Any other conditions that would limit compliance with study requirements.
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History of myocardial infarction ≤ 6 months prior to registration, or congestive heart failure requiring use of ongoing maintenance therapy for life-threatening ventricular arrhythmias.
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Other active malignancy ≤ 3 years prior to registration.
- EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix.
- NOTE: If there is a history of prior malignancy, they must not be receiving other specific treatment for their cancer.
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Unresolved toxicity from prior chemotherapy (subjects must be recovery to ≤ grade 1 toxicity from previous anticancer treatments or previous investigational agents).
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Receiving any other investigational agent or device ≤ 14 days prior to registration.
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Planning on receiving other medical, surgical, or radiological cancer treatments during the course of this study.
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Evidence of untreated fluid retention at the time of registration (including, for example, peripheral edema, pleural effusion, or ascites on physical or radiological examination) or history of severe capillary leak syndrome.
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Any other condition which the investigator believes would make participation in the study not acceptable.
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Subjects with any active and/or symptomatic brain metastases or active primary central nervous system (CNS) and subjects with carcinomatosis meningitis are excluded.
- NOTE: History of brain metastases treated by surgery and/or radiotherapy provided neurologically stable and off steroids ≥ 4 weeks prior to registration are allowed.
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Grade 2 or greater neuropathy (excluding diagnosed carpal tunnel syndrome).
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Use of concomitant medication that are known to be strong or moderate inhibitors or inducers of CYP3A4 and CYP2B6 ≤ 14 days prior to registration.
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Use of concomitant medication that are known to be substrates of CYP3A4, CYP2B6, or transporters of OAT3, MATE1, MATE2-K ≤ 14 days prior to registration.
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Corrected QT (QTc) prolongation based on QTc interval prior to registration of ≥ 470 ms using the Fridericia's formula (QTcF).
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Confluent superficial keratitis, a cornea epithelial defect, a corneal ulcer or stromal opacity.
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Significant electrolyte imbalance.
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Significant uncontrolled congestive heart failure.
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Symptomatic uncontrolled cardiac arrhythmia.
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Genetic predisposition for long QT syndrome.
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Subjects who are receiving concomitant QT prolonging medication.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: Treatment (MTI-301)
Patients receive MTI-301 PO QD on days 1-28 of each cycle. Cycles repeat every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT, PET/CT, or MRI and collection of blood samples throughout the study, and undergo tissue sample collection at baseline and at disease progression. |
Undergo MRI
Inne nazwy:
Ancillary studies Undergo CT or PET/CT
Inne nazwy:
Undergo PET/CT
Inne nazwy:
Undergo tissue and blood sample collection
Inne nazwy:
Given PO
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Maximum tolerated dose
Ramy czasowe: Up to 28 days (1 cycle)
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Will be defined as the dose level below the lowest dose that induces dose-limiting toxicity (DLT) in at least one-third of patients (at least 2 of a maximum of 6 new patients). DLT will be defined as an adverse event attributed as definitely, probably, or possibly related to MTI-301. |
Up to 28 days (1 cycle)
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Incidence of adverse events
Ramy czasowe: Up to 30 days after last dose of study treatment
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Will be graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. The number and severity of all adverse events (overall, by dose-level, and by tumor group) will be tabulated and summarized. Grade 3+ adverse events will be described and summarized in a similar fashion. This will provide an indication of the level of tolerance for this treatment combination. |
Up to 30 days after last dose of study treatment
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Objective response rate
Ramy czasowe: Up to 6 cycles (1 cycle = 28 days)
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Will be defined as the proportion of patients who achieve complete response (CR) or partial response (PR) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 during protocol treatment (up to maximum of 6 cycles of treatment) among treated patients. |
Up to 6 cycles (1 cycle = 28 days)
|
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Duration of response
Ramy czasowe: Up to 1 year
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Will be defined as the time from the date of first documented CR or PR to the date of first documented disease progression or death due to all causes, whichever occurs first. |
Up to 1 year
|
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Progression free survival
Ramy czasowe: Up to 1 year
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Will be defined as the time from the date of registration to the date of first documented disease progression or death due to all causes, whichever occurs first. |
Up to 1 year
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Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Winston Tan, MD, Mayo Clinic
Publikacje i pomocne linki
Przydatne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Procesy patologiczne
- Nowotwory
- Procesy Nowotworowe
- Stany patologiczne, oznaki i objawy
- Przerzuty nowotworu
- Techniki śledcze
- Techniki laboratoryjne kliniczne
- Techniki i procedury diagnostyczne
- Diagnoza
- Techniki chemii, analityczne
- Analiza widma
- Prowadzenie okazów
- Spektroskopia rezonansu magnetycznego
Inne numery identyfikacyjne badania
- MC210103
- MC210103 (Inny identyfikator: Mayo Clinic)
- NCI-2025-01930 (Identyfikator rejestru: CTRP (Clinical Trial Reporting Program))
- 24-012791 (Inny identyfikator: Mayo Clinic Institutional Review Board)
- R44CA272064 (Grant/umowa NIH USA)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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