- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07614022
A Study of LP-118 In Combination With Ponatinib, Dexamethasone And Blinatumomab For Adults With Newly-Diagnosed, BCR::ABL1-Positive Acute Lymphoblastic Leukemia (ALL)
A Phase I Study of the Bcl-2/Bcl-XL Inhibitor LP-118 In Combination With Ponatinib, Dexamethasone And Blinatumomab For Adults With Newly-Diagnosed, Philadelphia-Chromosome/BCR::ABL1-Positive Acute Lymphoblastic Leukemia
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Philadelphia-Chromosome/BCR::ABL1-Positive (Ph+) acute lymphoblastic leukemia (ALL) is a type of blood cancer that happens when a specific genetic change occurs in the DNA of certain blood cells, leading to uncontrolled growth of cells. Ph+ ALL is a more aggressive form of leukemia compared to other types but with specific medications called tyrosine kinase inhibitors, treatment outcomes have significantly improved. Unfortunately, some patients still do experience relapsed disease, when their leukemia comes back after treatment, which is challenging to treat. Therefore, research is ongoing to determine ways to improve therapy and outcomes for patients with Ph+ ALL.
The purpose of this study is to learn more about LP-118 and its side effects and decide on acceptable doses when combined with Food and Drug Administration (FDA) approved therapy for adult patients with Ph+ ALL. All participants will receive standard of care treatment for newly diagnosed Ph+ ALL consisting of the FDA approved drugs ponatinib, dexamethasone, intrathecal (injection into the spinal canal, also called "spinal tap") and systemic methotrexate and blinatumomab. This study will investigate different dose levels of LP-118 when given with his treatment combination to determine the most effective doses that can be safely given to patients with Ph+ ALL. This means that enrolled patients will receive progressive increasing or decreasing doses of LP-118 until the highest effective and safe dose is determined, while closely monitoring patients for any side effects or reactions. The highest dose is the dose that is the most effective dose that can be safely given to patients. This study will also preliminarily investigate if the addition of LP-118 improves treatment responses and outcomes for patients. If this trial is successful, the effectiveness of LP-118 added to this treatment regimen to treat Ph+ ALL will be studied in the next phase of clinical trials.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
- Navn: Dianna Auman, RN
- Telefonnummer: 336-716-1122
- E-mail: Dianna.Roesler@Advocatehealth.org
Studiesteder
-
-
North Carolina
-
Charlotte, North Carolina, Forenede Stater, 28204
- Atrium Health Levine Cancer
-
Kontakt:
- Katarzyna Wydrzynska-Gruner, RN
- Telefonnummer: 704-355-2000
- E-mail: katarzyna.wydrzynskagruner@advocatehealth.org
-
Underforsker:
- Thomas Knight, MD
-
Winston-Salem, North Carolina, Forenede Stater, 27157
- Atrium Health Wake Forest Baptist Comprehensive Cancer Center
-
Ledende efterforsker:
- Madelyn Burkart, MD
-
Kontakt:
- Dianna Auman, RN
- Telefonnummer: 336-716-1122
- E-mail: Dianna.Roesler@Advocatehealth.org
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Ability to understand and willingness to sign an IRB-approved informed consent.
- Age ≥ 18 years at the time of consent.
- ECOG Performance Status (PS) ≤ 2.
- Histological or cytological confirmation of newly diagnosed CD19-positive Philadelphia-chromosome/BCR::ABL1-positive ALL.
- Creatinine clearance: ≥60 mL/min, determined by the Cockroft-Gault formula, or measured by a 24-hour urine collection.
- Bilirubin ≤ 1.5 × upper limit of normal (ULN) - Unless liver abnormalities considered due to Gilbert's syndrome or of non-hepatic origin i.e., leukemic involvement. For patients with Gilbert's syndrome, bilirubin ≤1.5 x of their baseline bilirubin level will be required.
- Aspartate aminotransferase (AST) - Unless liver abnormalities considered due to Gilbert's syndrome or of non-hepatic origin i.e., leukemic involvement. For patients with Gilbert's syndrome, bilirubin ≤1.5 x of their baseline bilirubin level will be required.
- Alanine aminotransferase (ALT) - Unless liver abnormalities considered due to Gilbert's syndrome or of non-hepatic origin i.e., leukemic involvement. For patients with Gilbert's syndrome, bilirubin ≤1.5 x of their baseline bilirubin level will be required.
- Individuals of childbearing potential (ICBP) must have a negative serum pregnancy test. NOTE: Individuals who may become pregnant are considered to have childbearing potential unless they are surgically infertile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or are postmenopausal (at least 12 consecutive months with no menses without an alternative medical cause).
- ICBP must be willing to use two forms of contraception, one of which must be a barrier method and the other must be a highly effective contraceptive method from the time of informed consent until 6 months after study treatment discontinuation. Male participants with female partners of reproductive potential will need to agree to use contraception methods described above during study treatment and for at least 6 months after completion of all study treatment.
- Male participants must agree to refrain from sperm donation during study treatment and for at least 6 months after completion of all study treatment.
- Ability to ingest oral medications without a malabsorption condition, known dysphagia, short-gut syndrome, gastroparesis, or other conditions that may limit the ingestion or gastrointestinal absorption, distribution, metabolism and excretion of drugs administered orally, per the enrolling investigator.
Exclusion Criteria:
- Any prior treatment for ALL except for a single dose of intrathecal (IT) chemotherapy, corticosteroids, hydroxyurea, a single dose of vincristine, cytarabine, leukapheresis, and/or a BCR::ABL1-targeted tyrosine kinase inhibitor. Permitted prior treatment is limited to a duration of no longer than 14 days. Permitted prior treatment must be stopped at least 24 hours prior to starting study therapy.
- Women who are pregnant, nursing, or who plan to become pregnant while in the study and for at least 6 months after the last administration of all study treatment. NOTE: breast milk cannot be stored for future use while the mother is being treated on study. Pregnant participants are excluded from this study because ponatinib, blinatumomab, and methotrexate have the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with ponatinib, blinatumomab, and methotrexate breastfeeding should be discontinued if the patient is treated with ponatinib, blinatumomab, and methotrexate.
- Active second malignancy except for localized prostate cancer, basal cell or squamous cell carcinoma of the skin and carcinoma in situ of the skin or cervix.
- Unstable or severe uncontrolled medical condition in the opinion of the enrolling investigator (e.g., unstable cardiac function or unstable pulmonary condition; uncontrolled infection).
- Participants with known history of hepatitis B virus, hepatitis C virus, or human immunodeficiency virus (HIV) are eligible if no evidence of active viral replication by blood testing (i.e. negative viral loads). HIV positive participants must be on active anti-retroviral therapy and willing to continue therapy during study treatment.
- Uncontrolled cardiac disease as determined by the enrolling investigator.
- Major surgery, as determined by the enrolling investigator, within 2 weeks before enrollment.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Combination of LP-118, ponatinib, dexamethasone, blinatumomab and methotrexate
LP-118 will be given as tablets of 10mg or 100mg during the induction II course only in combination with ponatinib, dexamethasone, methotrexate and blinatumomab. .
Ponatinib, dexamethasone and methotrexate dosing will remain fixed, whereas LP-118 dosing will be dependent on the dose level to which a participant is assigned.
|
s LP-118 dosing will be dependent on the dose level to which a participant is assigned:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Estimation of the Maximum Tolerated Dose (MTD) for LP-118 (Dose Escalation)
Tidsramme: The DLT monitoring period is from Day 1 of Course 2 until the end of Course 2 (approximately 21 days).
|
Binary variable indicating if a Dose Limiting Toxicity (DLT) occurred.
|
The DLT monitoring period is from Day 1 of Course 2 until the end of Course 2 (approximately 21 days).
|
|
Identification of the Recommended Phase 2 Dose (RP2D) LP-118 (Dose Expansion)
Tidsramme: The DLT monitoring period is from Day 1 of Course 2 until the end of Course 2 (approximately 21 days).
|
Binary variable indicating if a Dose Limiting Toxicity (DLT) occurred.
|
The DLT monitoring period is from Day 1 of Course 2 until the end of Course 2 (approximately 21 days).
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Overall Survival (OS).
Tidsramme: At most 10 years.
|
The time from treatment administration to death from any cause, or until last contact if the patient has not died
|
At most 10 years.
|
|
Event-Free Survival (EFS).
Tidsramme: At most 10 years.
|
Time from start of therapy until failure to achieve CR/CRi, relapse, or death from any cause or otherwise censored at the date of the last disease assessment.
|
At most 10 years.
|
|
Overall Complete Molecular Response (CMR) rate.
Tidsramme: At most 10 years.
|
Binary variable indicating if a CMR at any time while on study.
|
At most 10 years.
|
|
Measurable Residual Disease (MRD) rate.
Tidsramme: Approximately 3 years.
|
Binary variable indicating if MRD was achieved.
|
Approximately 3 years.
|
|
Complete clinical remission with incomplete count recovery (CRi)
Tidsramme: Approximately 3 years.
|
Complete clinical remission with incomplete count recovery (CRi) defined as complete clinical remission except with ANC< 1000/μL and/or platelets <100,000/μL
|
Approximately 3 years.
|
|
Overall Response (OR) rate.
Tidsramme: Approximately 3 years.
|
A binary variable indicating if a CR or CRi was achieved.
|
Approximately 3 years.
|
|
Relapsed-Free Survival (RFS).
Tidsramme: At most 10 years.
|
Time from Complete Remission (CR) or Complete Remission with Incomplete Hematologic Recovery (CRi) to disease relapse or death (whichever occurs first) or otherwise censored at the date of the last disease assessment.
|
At most 10 years.
|
|
Isolated Central Nervous System (CNS) relapse rate.
Tidsramme: At most 10 years.
|
Binary variable indicating if isolated CNS relapse occurred.
|
At most 10 years.
|
|
Complete Response (CR) rate.
Tidsramme: Approximately 3 years.
|
Complete clinical remission defined as the disappearance of leukemia as indicated by <5% marrow blasts and the absence of peripheral blasts or extramedullary disease, with recovery of hematopoiesis defined by Absolute Neutrophil Count (ANC) ≥1000/μL and platelets ≥100,000/μL.
|
Approximately 3 years.
|
|
Occurrence of toxicities per Common Terminology Criteria V5.0
Tidsramme: Approximately 3 years.
|
Binary variables indicating the occurrence of toxicities per Common Terminology Criteria V5.0.
|
Approximately 3 years.
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Madelyn Burkart, MD, Wake Forest University Health Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IRB00127277
- P30CA012197 (U.S. NIH-bevilling/kontrakt)
- ONC-LEUK-2405 (Anden identifikator: Atrium Health Wake Forest Baptist Comprehensive Cancer Center)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Philadelphia Positiv Akut Lymfoblastisk Leukæmi
-
H. Lee Moffitt Cancer Center and Research InstituteNovartisRekrutteringPhiladelphia kromosom positiv akut lymfoblastisk leukæmiForenede Stater
-
Novartis PharmaceuticalsAfsluttetPhiladelphia kromosom positiv CMLForenede Stater, Tyskland, Italien, Frankrig
-
Novartis PharmaceuticalsIkke rekrutterer endnuAkut lymfatisk leukæmi | Leukæmi, lymfoblastisk, akut, Philadelphia-positiv | Philadelphia kromosom positiv akut lymfoblastisk leukæmi
-
Bristol-Myers SquibbAfsluttetKronisk myeloid leukæmi | Philadelphia-positiv myeloid leukæmiBelgien, Holland, Spanien, Forenede Stater, Italien, Canada, Frankrig, Tyskland, Peru, Singapore, Det Forenede Kongerige, Australien, Sverige, Finland, Israel, Irland, Danmark, Korea, Republikken, Norge, Østrig, Sydafrika, Schweiz
-
Bristol-Myers SquibbAfsluttetKronisk myeloid leukæmi | Philadelphia-positiv myeloid leukæmiBelgien, Spanien, Forenede Stater, Italien, Argentina, Brasilien, Canada, Tyskland, Peru, Puerto Rico, Singapore, Sydafrika, Taiwan, Det Forenede Kongerige, Australien, Frankrig, Filippinerne, Sverige, Thailand, Den Russiske Føderation og mere
-
Chen SuningIkke rekrutterer endnu
-
Novartis PharmaceuticalsAfsluttetPhiladelphia kromosom positiv kronisk myelogen leukæmiTyskland, Canada, Frankrig, Spanien, Italien
-
The First Affiliated Hospital of Soochow UniversityIkke rekrutterer endnuPhiladelphia-positiv ALLEKina
-
Rambam Health Care CampusMiltenyi Biomedicine GmbHUkendtPhiladelphia kromosom-positiv kronisk myelocytisk leukæmiIsrael
-
PETHEMA FoundationAfsluttetPhiladelphia kromosom-negativ eller BCR-ABL-negativ, CD19-positiv ALLSpanien
Kliniske forsøg med LP-118
-
Newave Pharmaceutical IncRekrutteringAkut myeloid leukæmi | Myelomatose | Myelofibrose | Kronisk lymfatisk leukæmi | Non Hodgkin lymfom | Akut lymfatisk leukæmi | Myelodysplastisk/myeloproliferativ neoplasma | Lille lymfatisk lymfom | Kronisk myelomonocytisk leukæmi-2 | Richter transformation | T-celle-prolymfocytisk leukæmi | Myeodysplastisk syndrom | Myelodysplastisk neoplasma i blastfaseForenede Stater
-
Guangzhou Lupeng Pharmaceutical Company LTD.AfsluttetLymfom, Non-Hodgkin | Solid tumorKina
-
Bausch Health Americas, Inc.Dow Pharmaceutical SciencesAfsluttetPlaque PsoriasisForenede Stater
-
Vertex Pharmaceuticals IncorporatedAfsluttetCystisk fibroseForenede Stater
-
Bausch Health Americas, Inc.Dow Pharmaceutical SciencesAfsluttetPlaque PsoriasisForenede Stater
-
AbbVieKU Leuven; Syndesi TherapeuticsAfsluttet
-
Bausch Health Americas, Inc.Dow Pharmaceutical SciencesAfsluttetPlaque PsoriasisForenede Stater
-
Addpharma Inc.Ikke rekrutterer endnuKronisk hjertesvigtSydkorea
-
InQpharm GroupAfsluttetBlodtryk | Low Density Lipoprotein KolesterolniveauTyskland
-
Shanxi Kangbao Biological Product Co., Ltd.Institute of Pathogen Biology, Beijing, ChinaRekruttering