SMD Clinical Trial
— AcadesineOfficial title:
A Phase I-II Trial of Acadesine in IPSS High and Int-2 SMD, LAM With 20-30% Marrow Blasts and CMML Type 2 Not Responding to Azacitidine or Decitabine for at Least 6 Courses or Relapsing After a Response
A phase I-II trial of Acadesine in IPSS high and int 2 myelodysplastic syndromes, acute
myeloid leukemia with 20-30% marrow blasts and chronic myelomonocytic leukemia type 2 not
responding to Azacitidine or Decitabine for at least 6 courses or relapsing after a
response:
Patients will receive 6 treatment cycles unless disease progression, transformation, or
unacceptable toxicity occurs, or the patient refuses to continue participating in the study.
Efficacy will be assessed at the end of the 2nd, 4th and 6th cycles. After 6 cycles,
patients demonstrating a response (CR, PR, marrow CR, or HI) will be able to continue with
cycles of Acadesine (at the same dose as in the preceding cycles, depending on their cohort)
until progression.
| Status | Terminated |
| Enrollment | 5 |
| Est. completion date | June 2015 |
| Est. primary completion date | June 2013 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Myelodysplastic syndrome including the following WHO categories: refractory anemia with excess blasts (RAEB), non-proliferative chronic myelomonocytic leukemia (CMML) (leukocytes < 13 G/L but > 10% marrow blasts), WHO- AML with 20-30% marrow blasts (RAEB-T according to the FAB classification) - Prior treatment with Azacitidine or Decitabine for at least 6 courses without response (including CR, PR, marrow CR and stable disease with hematological improvement) or relapse after a response - IPSS score >1 (IPSS: Int-2 or High); - Age = 18 years; - Normal liver function tests, defined by total bilirubin and transaminases less than 1.5 time the upper limit of normal; - Normal renal function, defined by creatinine less than 1.5 time the upper limit of normal, creatinine clearance = 50 mL/min. - Patient ineligible for allogeneic hematopoietic stem cell transplantation; - 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 between 0-2 at the time of screening; - Women of childbearing potential must: Agree to use effective contraception without interruption throughout the study and for a further 1 month after the end of treatment; - Men must: Agree to not conceive during the treatment and to use effective contraception during the treatment period (including periods of dose reduction or temporary suspension) and for a further 1 month after the end of treatment if their partner is of childbearing potential. Exclusion Criteria: - 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 30 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 study entry with the exception of hydroxyurea. The patient must have recovered from all acute toxicities from any previous therapy. - 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; - 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 allotransplantation. - Known allergy to acadesine or any of its excipients - No affiliation to an insurance system |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| France | Centre hospitalier de la côte Basque | Bayonne | |
| France | Hôpital Avicenne | Bobigny | |
| France | CHU de Haut-Lévèque | Bordeaux Pessac | |
| France | Centre henri Mondor | Creteil | |
| France | CHU de Grenoble | Grenoble | |
| France | CHU de Limoges | Limoges | |
| France | Institut paoli calmettes | Marseille | |
| France | centre hospitalier de Meaux | Meaux | |
| France | CHU de nantes | Nantes | |
| France | Centre Antoine Lacassagne | Nice | |
| France | Hôpital L'archet 1, Nice | Nice | |
| France | Hôpital Cochin | Paris | |
| France | Hôpital Saint Antoine | Paris | |
| France | Hôpital Saint Louis | Paris | |
| France | Hôpital Saint-Louis | Paris | |
| France | Centre henri Becquerel | Rouen | |
| France | Hôpital Bretonneau de Tours | Tours |
| Lead Sponsor | Collaborator |
|---|---|
| Groupe Francophone des Myelodysplasies | Advancell - Advanced In Vitro Cell Technologies, S.A. |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Determine the maximal tolerated dose (MTD) | Phase I: Evaluation after 6 month of treatment. Responders will be treated until progression | 6 month of treatment | Yes |