- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07609823
A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL
29 juillet 2026 mis à jour par: 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.
Aperçu de l'étude
Statut
Recrutement
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
75
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Jianyong Li
- Numéro de téléphone: 025-83781120
- E-mail: lijianyonglm@126.com
Lieux d'étude
-
-
Jiangsu
-
Nanjing, Jiangsu, Chine
- Recrutement
- The First Affiliated Hospital of Nanjing Medical University
-
Contact:
- Huayuan Zhu
- Numéro de téléphone: 86-13813810650
- E-mail: huayuan.zhu@hotmail.com
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
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.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
|
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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
Délai: Up to approximately 28 months
|
Up to approximately 28 months
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
ORR assessed by Investigator(INV)
Délai: Up to approximately 28 months
|
Up to approximately 28 months
|
|
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
Délai: Up to approximately 28 months
|
Up to approximately 28 months
|
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Time to response (TTR) assessed by IRC and INV, respectively
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Duration of response (DOR) assessed by IRC and INV, respectively
Délai: Up to approximately 30 months.
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Up to approximately 30 months.
|
|
Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
Délai: Up to approximately 28 months
|
Up to approximately 28 months
|
|
Progression-free survival (PFS) assessed by IRC and INV, respectively
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Overall Survival
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse events(AEs) as assessed by CTCAE v5.0
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Adverse drug reactions (ADRs) related to Lacutoclax
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Serious adverse events (SAEs)
Délai: Up to approximately 30 months
|
Up to approximately 30 months
|
|
Maximum Plasma Concentration(Cmax)
Délai: 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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Time to Maximum Plasma Concentration (Tmax)
Délai: 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)
Délai: From 1 hour prior to administration to 24 hours post-dose
|
From 1 hour prior to administration to 24 hours post-dose
|
|
Area Under the Plasma Concentration-Time Curve from Time Zero to Time t(AUC0-t)
Délai: 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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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
14 juillet 2026
Achèvement primaire (Estimé)
30 mars 2028
Achèvement de l'étude (Estimé)
30 septembre 2029
Dates d'inscription aux études
Première soumission
20 mai 2026
Première soumission répondant aux critères de contrôle qualité
20 mai 2026
Première publication (Réel)
27 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
30 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
29 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Processus pathologiques
- Tumeurs
- Maladie chronique
- Attributs de la maladie
- Maladies du système immunitaire
- Tumeurs par type histologique
- Maladies hématologiques
- Maladies lymphatiques
- Troubles lymphoprolifératifs
- Troubles immunoprolifératifs
- Leucémie, cellule B
- Leucémie, Lymphoïde
- Leucémie
- Conditions pathologiques, signes et symptômes
- Maladies hémiques et lymphatiques
- Récurrence
- Leucémie lymphocytaire chronique à cellules B
Autres numéros d'identification d'étude
- LP-10821
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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