- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01032148
Study of LBH589, A Deacetylase Inhibitor in Patients With Recurrent or Refractory Hodgkin or Non-Hodgkin's Lymphoma
11 januari 2017 uppdaterad av: Roswell Park Cancer Institute
Phase I Study of LBH589, A Novel Oral Deacetylase Inhibitor in Patients With Recurrent or Refractory Hodgkin or Non-Hodgkin's Lymphoma
The purpose of this study is to find out the effects of a drug called LBH589 when given to people with recurrent or refractory Hodgkin or Non-Hodgkin's lymphoma.
The safety of this drug will also be studied.
The participants' physical state, changes in the size of the tumor, or state of Hodgkin or non-Hodgkin's Lymphoma, and laboratory findings taken while on-study will help the researchers decide if LBH589 is safe and effective.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is an open-label, standard 3-3 dose finding scheme with a modification that allows intra-patient dose modification to determine maximum tolerated dose and toxicity profile of LBH589 in patients with recurrent or refractory Hodgkin's or non-Hodgkin's lymphoma.
Studietyp
Interventionell
Inskrivning (Faktisk)
8
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
New York
-
Buffalo, New York, Förenta staterna, 14263
- Roswell Park Cancer Institute
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Male or female patients age ≥ 18 years old with relapsed/refractory Hodgkin lymphoma or NHL patients who have relapsed or are refractory after receiving a minimum of two prior therapies
- Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
Laboratory requirements:
- ANC ≥ 1.5 x 10(9th)/L, unless due to bone marrow involvement with lymphoma
- Hemoglobin ≥ 9 g/dl without packed red blood cell dependency, unless due to bone marrow involvement with lymphoma
- Platelets ≥ 100 x 10(9th)/L, unless due to bone marrow involvement with lymphoma
- Serum creatinine ≤ 1.5 x Upper limit of Normal, or calculated Creatinine Clearance ≥ 50 mL/min
- AST and ALT ≤ 2.5 x Upper limit of Normal, unless due to liver involvement with lymphoma
- Serum bilirubin ≤ 1.5 x Upper limit of Normal
- Albumin > 3.0 g/dl
- Serum potassium ≥ Lower limit of Normal
- Total serum calcium [corrected for serum albumin] or ionized calcium ≥ Lower limits of normal
- Serum magnesium ≥ Lower limit of Normal
- Serum phosphorus ≥ Lower limit of Normal
- TSH ≥ LLN and free T4 within normal limits. Patients are permitted to receive thyroid hormone supplements to treat underlying hypothyroidism.
- Baseline MUGA or ECHO must demonstrate LVEF ≥ 50%
- ECOG Performance Status of ≤ 2
Exclusion Criteria:
- Prior HDAC, DAC, HSP90 inhibitors or valproic acid for the treatment of cancer
- Patients who will need valproic acid for any medication during the study or within 5 days prior to first LBH589 treatment
- Peripheral neuropathy ≥ CTCAE grade 1
- Impaired cardiac function or clinically significant cardiac diseases, including any one of the following:
- Patients with congenital QT syndrome
- History or presence of sustained ventricular tachyarrhythmia.
- Any history of ventricular fibrillation or torsade de pointes
- Bradycardia defined as Heart Rate < 50 bpm. Patients with pacemakers are eligible if Heart Rate ≥ 50 bpm
- Screening EKG with a QTc.450msec
- Right Bundle branch block + left anterior hemiblock (bifascicular block)
- Patients with myocardial infarction or unstable angina ≤ 6 months prior to starting study drug
- other clinically significant heart disease (e.g. CHF NY Heart Association class III or IV, uncontrolled hypertension, history of labile hypertension or history of poor compliance with an antihypertensive regimen)
- Impairment of GI function or GI disease that may significantly alter the absorption of LBH589
- Patients with Diarrhea > CTCAE grade 1
- Other concurrent severe and/or uncontrolled medical conditions (e.g. uncontrolled diabetes or active or uncontrolled infection) including abnormal laboratory values that could cause unaccepted safety risks or compromise compliance with the protocol
- Patients using medications that have a relative risk of prolonging the QT interval or inducing torsade de pointes if treatment cannot be discontinued or switched to a different medication prior to starting study drug
- Concomitant use of CYP3A4 inhibitors
- Patients who have received targeted agents within 2 weeks or within 5 half-lives of the agent and active metabolites(which ever is longer) and who have not recovered from side effects of those therapies
- Patients who have received either immunotherapy within ≤ 8 weeks;chemotherapy within ≤ 4 weeks or radiation therapy to >30% of marrow-bearing bone within ≤ weeks prior to starting study treatment or who have not yet recovered from side effects of such therapies
- Patients with an active bleeding tendency or is receiving any treatment with therapeutic doses of sodium warfarin or coumadin derivatives. Low doses of Coumadin (e.g.≤2 mg/day) to maintain line patency is allowed.
- Patients who have undergone major surgery ≤ 4 weeks prior to starting study drug or who have not recovered from side effects of such therapy
- Women who are pregnant or breast feeding or women of childbearing potential not using effective method of birth control
- Male patients whose sexual partners are women of childbearing potential not using effective birth control
- Patients with prior malignancy within 5 years (except for basal or squamous cell carcinoma, in situ cancer of the cervix or early stage prostate or bladder carcinomas)
- Patients with known positivity for HIV or hepatitis C: baseline testing for HIV and Hepatitis C is not required
- Prior allogenic stem cell transplant
- Patients with any significant history of non-compliance to medical regimens or unwilling or unable to comply with the instructions given to him/her by the study staff
- Patients taking CYP2D6 inhibitors should be carefully monitored, but these drugs are not necessarily contraindicated when use concomitantly with LBH. Use of these drugs is not an exclusion criterion
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: LBH589
LBH589 administered orally as once daily dose of 20 mg po q M, W, F on a q 28 day cycle, escalating to a maximum dase of 60 mg
|
LBH589 will be administered orally as once daily dose of 20 mg po q M, W, F on a q28 day cycle.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Determine maximum tolerated dose (MTD) of LBH589
Tidsram: 2 years
|
2 years
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Determine toxicity profile in study population
Tidsram: 28 days after Cycle 2 Day 1
|
28 days after Cycle 2 Day 1
|
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Determine anti-lymphoma activity of LBH589 in (non-CTCL) Hodgkin's and non-Hodgkin's lymphoma patients
Tidsram: 2 Years
|
2 Years
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Francisco Hernandez, MD, Roswell Park Cancer Institute
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 december 2009
Primärt slutförande (Faktisk)
1 januari 2017
Avslutad studie (Faktisk)
1 januari 2017
Studieregistreringsdatum
Först inskickad
14 december 2009
Först inskickad som uppfyllde QC-kriterierna
14 december 2009
Första postat (Uppskatta)
15 december 2009
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
12 januari 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
11 januari 2017
Senast verifierad
1 januari 2017
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
- Immunsystemets sjukdomar
- Neoplasmer efter histologisk typ
- Neoplasmer
- Lymfoproliferativa störningar
- Lymfatiska sjukdomar
- Immunproliferativa störningar
- Lymfom
- Lymfom, icke-Hodgkin
- Molekylära mekanismer för farmakologisk verkan
- Enzyminhibitorer
- Antineoplastiska medel
- Histon deacetylashämmare
- Panobinostat
Andra studie-ID-nummer
- RPCI I 147408
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .