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- Klinische proef NCT07609823
A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL
29 juli 2026 bijgewerkt door: Guangzhou Lupeng Pharmaceutical Company LTD.
A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL).
Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W.
Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs).
This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.
Studie Overzicht
Toestand
Werving
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Geschat)
75
Fase
- Fase 2
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studiecontact
- Naam: Jianyong Li
- Telefoonnummer: 025-83781120
- E-mail: lijianyonglm@126.com
Studie Locaties
-
-
Jiangsu
-
Nanjing, Jiangsu, China
- Werving
- The First Affiliated Hospital of Nanjing Medical University
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Contact:
- Huayuan Zhu
- Telefoonnummer: 86-13813810650
- E-mail: huayuan.zhu@hotmail.com
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-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Nee
Beschrijving
Inclusion Criteria:
- Patients with confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
- Patients who had previously received standard therapy, experienced disease progression following the most recent line of treatment (excluding intolerance), and had at least one indication for treatment prior to enrollment.
- Have at least one measurable lesion.
- Age ≥18 years, regardless of sex.
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
- Life expectancy ≥ 12 weeks.
- Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
- Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
- Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of Lacutoclax. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose of Lacutoclax.
- Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.
Exclusion Criteria:
- Known hypersensitivity to Lacutoclax or any of its excipients.
- Prior treatment with a BCL-2 family inhibitor.
- History of or currently suspected Richter's syndrome.
- Known or suspected central nervous system (CNS) involvement.
- Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
- Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
- Received corticosteroids for antitumor purposes, herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
- Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to dosing.
- Prior malignancy other than CLL/SLL within the past 2 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
- Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
- Presence of any severe and/or uncontrolled systemic disease.
- Impaired cardiac function.
- Any uncontrolled systemic infection.
- Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
- Unable to discontinue moderate or strong CYP3A inhibitors or inducers, or sensitive CYP2C8 substrates during the study period.
- Primary autoimmune disease requiring immunosuppressive therapy.
- Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
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: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
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Participants will first undergo a dose ramp-up period of at least 4 days (Cycle 0: C0D1-C0D4), followed by continuous administration at the target dose of 400 mg once daily starting from Cycle 1.
Each treatment cycle will last 28 days.
Treatment will continue until disease progression, unacceptable toxicity, or fulfillment of other criteria for treatment discontinuation.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
Tijdsspanne: Up to approximately 28 months
|
Up to approximately 28 months
|
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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ORR assessed by Investigator(INV)
Tijdsspanne: Up to approximately 28 months
|
Up to approximately 28 months
|
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Complete response(CR) plus complete response with incomplete bone marrow recovery (CRi) rate (CRi applicable only to patients with CLL) assessed by IRC and INV, respectively
Tijdsspanne: Up to approximately 28 months
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Up to approximately 28 months
|
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Time to response (TTR) assessed by IRC and INV, respectively
Tijdsspanne: Up to approximately 30 months
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Up to approximately 30 months
|
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Duration of response (DOR) assessed by IRC and INV, respectively
Tijdsspanne: Up to approximately 30 months.
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Up to approximately 30 months.
|
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Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
Tijdsspanne: Up to approximately 28 months
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Up to approximately 28 months
|
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Progression-free survival (PFS) assessed by IRC and INV, respectively
Tijdsspanne: Up to approximately 30 months
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Up to approximately 30 months
|
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Overall Survival
Tijdsspanne: Up to approximately 30 months
|
Up to approximately 30 months
|
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Adverse events(AEs) as assessed by CTCAE v5.0
Tijdsspanne: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse drug reactions (ADRs) related to Lacutoclax
Tijdsspanne: Up to approximately 30 months
|
Up to approximately 30 months
|
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Serious adverse events (SAEs)
Tijdsspanne: Up to approximately 30 months
|
Up to approximately 30 months
|
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Maximum Plasma Concentration(Cmax)
Tijdsspanne: From 1 hour prior to administration to 24 hours post-dose
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From 1 hour prior to administration to 24 hours post-dose
|
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Time to Maximum Plasma Concentration (Tmax)
Tijdsspanne: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
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Half-life (T1/2)
Tijdsspanne: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
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Area Under the Plasma Concentration-Time Curve from Time Zero to Time t(AUC0-t)
Tijdsspanne: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
14 juli 2026
Primaire voltooiing (Geschat)
30 maart 2028
Studie voltooiing (Geschat)
30 september 2029
Studieregistratiedata
Eerst ingediend
20 mei 2026
Eerst ingediend dat voldeed aan de QC-criteria
20 mei 2026
Eerst geplaatst (Werkelijk)
27 mei 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
30 juli 2026
Laatste update ingediend die voldeed aan QC-criteria
29 juli 2026
Laatst geverifieerd
1 juli 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Pathologische processen
- Neoplasmata
- Chronische ziekte
- Ziekte attributen
- Ziekten van het immuunsysteem
- Neoplasmata per histologisch type
- Hematologische ziekten
- Lymfatische ziekten
- Lymfoproliferatieve aandoeningen
- Immunoproliferatieve aandoeningen
- Leukemie, B-cel
- Leukemie, Lymfoïde
- Leukemie
- Pathologische aandoeningen, tekenen en symptomen
- Hemische en lymfatische ziekten
- Herhaling
- Leukemie, lymfatische, chronische, B-cel
Andere studie-ID-nummers
- LP-10821
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .