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Active, not recruiting Phase 2

IDH1 (AG 120) Inhibitor in Patients With IDH1 Mutated Myelodysplastic Syndrome

NCT03503409 · tracked via the Priya Life Science France tracker
Phase
Phase 2
Started
2019-05-14
Last updated
2026-08-10

Condition(s) studied

Myelodysplastic SyndromesAcute Myeloid Leukemia

Investigational drug(s) / intervention(s)

AG-120 →

AG-120: 500 mg/day Oral of AG-120. AG-120 will be dispensed on Day 1 of each treatment cycle

Study summary

patients with MDS (Myelodysplastic Syndrome) and mutated IDH1 patients will be treated with AG120 (IDH1 inhibitor)

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients must meet all of the following criteria to participate in the study: * Age ≥ 18 years * Myelodysplastic syndrome according to WHO classification including non-proliferative AML up to 29% of BM blast * Belonging to one of the following categories : * higher risk (IPSS high or int 2 ) MDS without response to azacitidine (CR,PR, stable disease with HI) after at least 6 cycles , or relapsing after a response but without overt progression (defined by at least doubling of marrow blasts, compared to pre azacitidine bone marrow, or AML progression beyond 30% blasts) * Untreated higher risk MDS (IPSS int-2, high) without life threatening cytopenia including ANC \<500/mm3 or any recent severe infections and /or platelets below 30,000/mm3 or any bleeding symptom * lower risk MDS with resistance or loss of response to a previous treatment with epoetin alpha/ beta (≥60000 U/w) or Darbopoetin (≥250 ug/w) given for at least 12 weeks and RBC transfusion requirement at least 2 U/8 weeks in the previous 16 weeks * Presence of IDH1 mutation in either blood or marrow prior to start of therapy; * Normal renal function, defined by creatinine less than 1.5 times the upper limit of normal, creatinine clearance (Modification of diet in renal disease) creatinine clearance ≥ 50 mL/min; * Normal liver function, defined by total bilirubin and transaminases less than 1.5 times the upper limit of normal; * Adequate cardiac ejection fraction (\>40%); * Patient is not known to be refractory to platelet transfusions; * Written informed consent; * Patient must understand and voluntarily sign consent form. * Patient must be able to adhere to the visit schedule as outlined in the study and follow protocol requirements; * ECOG performance status 0-2 at the time of screening; * Female subjects with reproductive potential must have a negative serum pregnancy test within 7 days prior to the start of therapy. Subjects with reproductive potential are defined as sexually mature women who have not undergone a hysterectomy, bilateral oophorectomy or tubal occlusion or who have not been naturally postmenopausal (i.e., who have not menstruated at all) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months). Females of reproductive potential as well as fertile men and their partners who are female of reproductive potential must agree to abstain from sexual intercourse or to use two highly effective forms of contraception from the time of giving informed consent, during the study and for 3 months (females and males) following the last dose of AG-120. A highly effective form of contraception is defined as hormonal oral contraceptives, injectables, patches, intrauterine devices. * Male patients must : * Agree the need for the use of a condom if engaged in sexual activity with a woman of childbearing potential during the entire period of treatment, even if disruption of treatment and during 3 months after end of treatment. * Agree to learn about the procedures for preservation of sperm before starting treatment Exclusion Criteria: * A patient meeting any of the following criteria is not eligible to participate in the study: * Severe infection or any other uncontrolled severe condition. * Significant cardiac disease - NYHA Class III or IV or having suffered a myocardial infarction in the last 6 months. * Less than 14 days since prior treatment with growth factors (EPO, G-CSF). * Use of investigational agents within 30 days or any anticancer therapy within 2 weeks before the study entry with the exception of hydroxyurea. The patient must have recovered from all acute toxicity from any previous therapy. * Subject has a heart-rate corrected QT interval using Fridericia's method (QTcF) ≥ 470 msec or any other factor that increases the risk of QT prolongation or arrhythmic events (e.g., heart failure, hypokalemia, family history of long QT interval syndrome). Subjects with prolonged QTcF interval in the setting of bundle branch block may participate in the study. * Subject is taking known strong cytochrome P450 (CYP) 3A4 inducers or inhibitors or sensitive CYP3A4 substrate medications with a narrow therapeutic window, unless they can be transferred to other medications within ≥ 5 half-lives prior to dosing. * Subject is taking P-glycoprotein (P-gp) transporter-sensitive substrate medications with a narrow therapeutic window, unless they can be transferred to other medications within ≥ 5 half-lives prior to administration of study treatment * Active cancer or cancer during the year prior to trial entry other than basal cell carcinoma, or carcinoma in situ of the cervix or breast. * Patient already enrolled in another therapeutic trial of an investigational drug. * Known HIV infection or active hepatitis B or C. * Women who are or could become pregnant or who are currently breastfeeding. * Any medical or psychiatric contraindication that would prevent the patient from understanding and signing the informed consent form. * Patient eligible for allogeneic stem cell transplantation. * Known allergies to AG 120 or any of its excipients. * The study does not provide for the inclusion of persons referred to in Articles L. 1121-5 to L. 1121-9 and L. 1122-1-2 of the Public Health Code (e.g. minors, protected adults, etc.) * No affiliation to a health insurance system.

Primary outcome measure(s)

  • Overall hematological response — 6 months
    overall hematological response

Trial sites (38)

FacilityCityRegionStatus
CH Angers Angers France
Centre Hospitalier de la Côte Basque Bayonne France
Hôpital Nord Franche-Comté/Service de médecine interne / Hématologie clinique Belfort France
CHU côte de Nacre Caen France
CHU de Grenoble/Clinique Universitaire d'hématologie 6e A Grenoble France
CH Le Mans/Service d'hématologie Oncologie Le Mans France
CHRU de Limoges Limoges France
centre hospitalier de Lyon Lyon France
Institut Paoli Calmettes/Unité d'Hématologie 3 Marseille France
CHU Montpellier St Eloi Montpellier France
Hôpital E. Muller-GHR Mulhouse Sud-Alsace Mulhouse France
CHU Hôtel Dieu/Service d'Hématologie Clinique Nantes France
Hôpital Archet 1/Service d'Hématologie Clinique Nice France
GHU Caremeau Nîmes France
Hôpital Saint Louis - Hématologie Séniors Paris France
Hôpital Necker Paris France
Hôpital Henri Mondor Paris France
CHU de Haut-Lévèque/Centre François Magendie/Service des maladies du sang Pessac France
CHU de Poitiers/Pôle de cancérologie - secteur tertiaire- Poitiers France
Centre Henri Becquerel Rouen France
institut de cancérologie Lucien Neuwirth Saint-Priest-en-Jarez France
Médecine Interne/IUCT Oncopole Toulouse France
CHU de Tours Tours France
CHU Brabois Vandœuvre-lès-Nancy France
Centre Hospitalier de Versailles-Hôpital André Mignot Versailles France
Ematologia ALESSANDRIA Alessandria Italy
CLINICA Ematologica ANCONA Ancona Italy
Ematologia BOLOGNA Bologna Italy
Ematologia BRESCIA Brescia Italy
Ematologia FIRENZE Florence Italy
Clinica Ematologica Genova Genova Italy
Ematologia GENOVA Genova Italy
Ematologia LECCE Lecce Italy
Ematologia MILANO Milan Italy
Ematologia ORBASSANO Orbassano Italy
Ematologia ed Immunologia Clinica PADOVA Padova Italy
Reggio Calabria Reggio Calabria Italy
Ematologia ROMA Roma Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03503409 on ClinicalTrials.gov ↗ ← All trials in France