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A Pilot Study of Pivanex, a Histone Deacetylase Inhibitor, in Patients With Chronic Lymphocytic Leukemia

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Ce qui est testé

Collecte de données

Qui peut participer

Maladie chronique+11

+ Maladies Hématologiques

+ Maladies du Système Immunitaire

À partir de 18 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Étude thérapeutique

Phase 2
Interventionnel
Date de début : mai 2004
Voir le détail du protocole

Résumé

Sponsor principalTitan Pharmaceuticals
Dernière mise à jour : 14 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Date de début de l'étude : 1 mai 2004

Date à laquelle le premier participant a commencé l'étude.

Rationale: Chronic lymphocytic leukemia (CLL) is a disease characterized by the accumulation of mature lymphocytes. These CLL lymphocytes are blocked from undergoing terminal differentiation and apoptosis. Patients with CLL have limited options for therapy, especially after the failure of standard chemotherapy regimens. Histone deacetylase inhibitors (HDACs) comprise a new class of drugs being evaluated in the treatment of various malignancies. In vitro data suggest that HDAC inhibition leads to terminal B-cell differentiation and may therefore play a therapeutic role in the treatment of CLL. Pivanex (pivaloyloxymethyl butyrate) is an HDAC inhibitor that has been shown to induce apoptosis of CLL lymphocytes in vitro. In previous clinical trials, Pivanex has been well tolerated. The goal of this protocol is to determine the effects of Pivanex in patients with CLL. Purpose: This open-label trial will determine the response rate of Pivanex in patients with CLL. Objectives: (1) Determine the response rate of Pivanex in patients with relapsed CLL; (2) Determine time to disease progression in patients with relapsed CLL treated with Pivanex; and (3) Determine the safety profile of Pivanex in CLL. Design: This is an open label, single arm, multiple dose, pilot study of patients with relapsed CLL. Patients will be treated with 2.5 g/m2 of Pivanex administered intravenously over 6 hours daily on Days 1 - 3. Treatment will be repeated every 21 days until disease progression or the patient is withdrawn from treatment for protocol-specified reasons. Disease status will be assessed prior to every odd-numbered treatment cycle using response criteria based upon the Revised National Cancer Institute-sponsored Working Group Guidelines for CLL. Patients withdrawn due to disease progression will be followed for survival. Patients withdrawn from study for reasons other than disease progression will be followed for disease progression and survival.

Titre officielA Pilot Study of Pivanex, a Histone Deacetylase Inhibitor, in Patients With Chronic Lymphocytic Leukemia 
Sponsor principalTitan Pharmaceuticals
Dernière mise à jour : 14 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

28 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Traitement

Cette étude teste un ou plusieurs traitements pour évaluer leur efficacité contre une maladie ou un problème de santé spécifique. L'objectif est de voir si un nouveau médicament ou une thérapie fonctionne mieux, ou provoque moins d'effets secondaires que les options existantes.


Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Tout sexe

Le sexe biologique des participants éligibles à s'inscrire.

À partir de 18 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains non autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Maladie chroniqueMaladies HématologiquesMaladies du Système ImmunitaireTroubles immunoprolifératifsLeucémieLeucémie lymphoïdeMaladies lymphatiquesTroubles LymphoprolifératifsNéoplasmes par type histologiqueNéoplasmesProcessus pathologiquesLeucémie à cellules BLeucémie lymphoïde chronique à cellules BAttributs de la maladie

Critères

Inclusion Criteria: * Patients must have a confirmed diagnosis of CLL or small lymphocytic lymphoma (SLL) based upon the Revised NCI-sponsored Working Group guidelines for CLL; * Relapsed or refractory disease after previous chemotherapy treatment; * Age \> 18 years; * Adequate renal function with creatinine \<= 1.5 mg/dL; * Adequate liver function with alkaline phosphatase \<= 2.5 X upper limit of normal, serum glutamic oxaloacetic transaminase (SGOT), and serum glutamic pyruvic transaminase (SGPT) \<= 2.5 X upper limit of normal; and total bilirubin \<= 2.0 X upper limit of normal; * Adequate bone marrow function as determined by having platelets \> 50,000/mm3 without transfusion in the preceding 2 weeks and an absolute neutrophil count (ANC) =\> 1,500 cells/mm3 without growth factor support; unless cytopenias due to marrow infiltration; * Able to give informed consent; * A minimum of 4 weeks must have elapsed from the completion of any previous treatment regimen, including radiation and biologic therapies (6 weeks if a prior nitrosourea or mitomycin C, 12 weeks if radioimmunotherapy) to treatment on Day 1 Cycle 1. Patients must have recovery from treatment-associated toxicity(ies); * A predicted life expectancy of at least 6 months; and * Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2. Exclusion Criteria: * More than three systemic treatment regimens for CLL/SLL (excluding immunotherapies and biologic therapies); * Concurrent malignancy that the patient has not been free of for at least 5 years, excluding curatively treated carcinoma-in-situ or non-melanoma skin cancer; * Any pregnant or lactating females. Females of childbearing potential must have a negative pregnancy test and all male and female patients of reproductive potential must agree to use adequate birth control; * Known HIV-positive patients; * Any underlying medical conditions or circumstances that would contraindicate therapy with study treatment, affect compliance or impair evaluation of study endpoints; * Receiving investigational agents within 4 weeks of the study treatment; and * Known allergy to reagents in the study.

Centres d'étude

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Cette étude comporte 1 site

Suspendu

Center for Lymphoma and Myeloma; Weill Medical College of Cornell University

New York, United StatesVoir le site
Suspendu1 Centres d'Étude