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- Klinische proef NCT07616089
Phase I Study of FXS0683 in the Treatment of Blood Tumors (FXS0683-001)
A Multicenter, Open, Single-arm Phase I Dose-escalation and Dose-expansion Clinical Study: Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of FXS0683 Tablets in Patients With Relapsed or Refractory Hematologic Malignancies.
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This is a first-in-human, multicenter, open-label, single-arm Phase I study of FXS0683 tablets in participants with relapsed or refractory hematologic malignancies, designed to evaluate safety, tolerability, PK, and preliminary antitumor activity.The study consists of a dose-escalation phase and a dose-expansion phase. The primary objective of dose escalation is to assess safety and tolerability and to determine the MTD and/or RP2D. Dose escalation will follow an accelerated titration design combined with a Bayesian Optimal Interval (BOIN) design. The initial cohort will enroll one participant; if a treatment-related adverse event of Grade ≥2 occurs during the dose-limiting toxicity (DLT) observation period, the cohort will transition to a BOIN design and expand to include additional participants. Dose escalation may proceed in the absence of DLTs among evaluable participants.
The dose-expansion phase is intended to further evaluate safety and preliminary efficacy at selected dose level(s). Expansion may be initiated based on emerging safety, tolerability, and PK data from the dose-escalation phase without requiring completion of all escalation cohorts.
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Lugui Qiu
- Telefoonnummer: 86 022-23608108
- E-mail: qiulg@ihcams.ac.cn
Studie Contact Back-up
- Naam: Bo Jiang
- Telefoonnummer: 86 022-23608381
- E-mail: jiangbo@ihcams.ac.cn
Studie Locaties
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Tianjin Municipality
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Tianjin, Tianjin Municipality, China, 301600
- Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences (IHCAMS)
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Contact:
- Shuo Chen
- Telefoonnummer: 86 022-23608381
- E-mail: gcp@ihcams.ac.cn
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Voluntary participation in the clinical trial and signing of the ICF.
- Age ≥ 18 years, regardless of gender.
- Dose escalation phase: Patients with mature B-cell malignancies diagnosed per the 2017 WHO classification who have failed standard therapies and have no appropriate treatment options. Dose expansion phase: Patients with B-cell lymphoma (2017 WHO), myeloid malignancies (2022 WHO), or acute lymphoblastic leukemia.
- Dose escalation phase: Evaluable disease. Dose expansion phase: For B-cell lymphoma, at least one measurable lesion per Lugano 2014 criteria.
- Patients must be willing to undergo bone marrow aspiration and/or biopsy.
- ECOG performance status of 0-1 (dose escalation phase) or 0-2 (dose expansion phase).
- Expected survival time ≥3 months.
- Adequate bone marrow function during screening, as defined by local laboratory reference ranges, without growth factor support.
- Adequate organ function, defined by laboratory values within 7 days prior to the first dose.
- Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose and agree to use effective contraception from signing the ICF until 6 months after the last dose.
- Patients at high risk of tumor lysis syndrome (TLS), defined as absolute lymphocyte count (ALC) ≥25×10⁹/L with ≥1 measurable lymph node ≥5 cm or any node ≥10 cm, must be willing to comply with TLS prophylaxis and monitoring requirements.
- Patients must be able to comply with the study procedures and visit schedule.
Exclusion Criteria:
- Burkitt lymphoma/leukemia, plasma cell myeloma, or plasmablastic lymphoma.
- Acute promyelocytic leukemia (APL) or BCR-ABL positive AML patients, or patients with a history of myeloproliferative neoplasms (MPN).
- Use of cytotoxic agents, investigational drugs, or other antitumor therapies within 14 days or 5 half-lives prior to the first dose; or immunotherapy, antibody-based or peptide-based therapies, or live vaccines within 4 weeks prior to the first dose.
- Patients who received any therapeutic surgery other than diagnosis, biopsy, or drainage within 4 weeks before the first dose, or patients expected to undergo major surgery during the study. Patients who underwent drainage or placement of drainage tubes within 4 weeks before the first dose must have symptoms/signs alleviated and not require prophylactic or therapeutic antibiotics.
- Patients who received systemic radiotherapy or palliative local radiotherapy within 4 weeks before the first dose.
- Toxicity from previous anticancer treatment has not recovered to ≤ grade 2, except for hair loss and pigmentation.
- Prior allogeneic stem cell transplantation; or autologous stem cell transplantation or CAR-T therapy within 3 months prior to the first dose.
- Patients with lymphoma/leukemia that has infiltrated the central nervous system.
- Patients with dysphagia or a history of severe gastrointestinal diseases and whose related symptoms cannot be reasonably controlled; or patients with gastrointestinal diseases affecting drug absorption or other malabsorption conditions.
- Active or clinically significant cardiovascular or cerebrovascular disease.
- Patients with interstitial lung disease or a history of pulmonary interstitial fibrosis; or evidence of active pneumonia found on screening chest CT scan.
- Patients with congenital immunodeficiency disorders or active autoimmune diseases, including but not limited to those with active and uncontrolled autoimmune cytopenias lasting ≥2 weeks, including autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura.
- Patients with coagulation disorders.
- Patients with a history of severe allergies or allergies to any active or inactive component of the study drug.
- Patients with uncontrolled systemic infections within 2 weeks before the first dose; hepatitis B surface antigen positive with hepatitis B virus DNA >1000 IU/ml; HCV antibody positive with HCV RNA positive; HIV antibody positive.
- Other primary malignancies within 5 years prior to enrollment, except for adequately treated basal or squamous cell skin cancer or carcinoma in situ.
- Patients who still require systemic immunosuppressive agents or systemic corticosteroids within 2 weeks before the study drug.
- Pregnant or breastfeeding women.
- Any other serious or uncontrolled acute or chronic disease or laboratory abnormality or other reasons deemed unsuitable for participation in this clinical trial by the investigator.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: FXS0683
This is a first-in-human, multicenter, open-label, single-arm Phase I study consisting of dose-escalation and dose-expansion phases.
FXS0683 will be administered orally once daily at assigned dose levels in 28-day cycles.
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FXS0683 is a potent and highly selective BCL-2 inhibitor
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Number of participants with DLTs
Tijdsspanne: At the end of Cycle 1 (each cycle is 28 days).
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A DLT is defined as any adverse event or laboratory abnormality occurring during the DLT observation period that is assessed as at least possibly related to FXS0683 and meets pre-specified DLT criteria, graded per NCI-CTCAE Version 6.0.
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At the end of Cycle 1 (each cycle is 28 days).
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MTD and/or RP2D
Tijdsspanne: Up to approximately 3 years.
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The MTD and/or RP2D will be determined based on the overall assessment of safety, tolerability, PK, and preliminary efficacy data.
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Up to approximately 3 years.
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Incidence and Severity of Adverse Events and Clinically Significant Safety Findings
Tijdsspanne: From first dose of study drug until 30 days after the last dose.
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Adverse events (AEs) will be summarized, and severity will be graded according to NCI-CTCAE Version 6.0.
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From first dose of study drug until 30 days after the last dose.
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Objective Response Rate (ORR) Of FXS0683 Monotherapy
Tijdsspanne: Up to approximately 3 years.
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ORR will be assessed according to disease-specific response criteria (e.g., Lugano 2014, iwCLL 2018, ELN 2022, or IWG 2006), as applicable.
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Up to approximately 3 years.
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Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata
- Ziekten van het immuunsysteem
- Neoplasmata per histologisch type
- Hematologische ziekten
- Lymfatische ziekten
- Lymfoproliferatieve aandoeningen
- Immunoproliferatieve aandoeningen
- Lymfoom, non-Hodgkin
- Lymfoom
- Leukemie, myeloïde
- Beenmergziekten
- Leukemie, Lymfoïde
- Leukemie
- Hemische en lymfatische ziekten
- Leukemie, myeloïde, acuut
- Lymfoom, B-cel
- Voorlopercel lymfoblastische leukemie-lymfoom
- Myelodysplastische syndromen
Andere studie-ID-nummers
- FXS0683-001
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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