A Phase I, Dose-escalation Study of AS703569 Given Orally to Subjects With Haematological Malignancies

Stopped early · Phase 1

Conditions studied: Haematological Malignancies

In brief

EMD Serono decided to terminate enrollment based on a review of the available clinical data and low probability of completing the trial based on the observed recruitment rate. Subjects already enrolled in the study continued participation in the study, consistent with the protocol, to study completion.

Key facts

Study ID

NCT01080664

Run by

EMD Serono

People needed

124

Starts

2006-12-01

Expected to finish

2011-08-01

Last updated by the study team

2013-10-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Dose-escalation part:
• Primary or secondary acute myeloid leukaemia, including subjects:
• with first or subsequent relapse after standard therapy, with no established treatment options; refractory to available therapies, e.g. who failed to achieve complete remission after chemotherapies; Newly-diagnosed elderly subjects (over 60 years) according to WHO classification (≥20 blasts in bone marrow), who did not accept or were not eligible for chemotherapy (first line therapy)
• Subjects with myelodysplastic syndrome (IPSS Int-2 or high risk) resistant or intolerant to standard treatment and not candidates for allogeneic HSCT.
• Subjects with chronic myeloid leukaemia in chronic, accelerated or blast-phase, resistant or intolerant to standard treatment and not candidates for allogeneic HSCT.
• Subjects with myeloproliferative disorders and no effective treatment options.
• Subjects with acute lymphoblastic leukaemia, relapsing, resistant or intolerant to standard treatment and no effective treatment options.
• Subjects with chronic lymphocytic leukaemia, relapsing, resistant or intolerant to standard treatment and no effective treatment options.
• Subjects with non-Hodgkin lymphoma, relapsing, resistant or intolerant to standard treatment with no effective treatment options.
• Cohort expansion part
• Primary or secondary acute myeloid leukaemia not eligible for chemotherapy (first line therapy), including subjects
• with first or subsequent relapse after standard therapy, for whom no established treatment options are available; refractory to available therapies, e.g. who failed to achieve complete remission after chemotherapies; Newly-diagnosed elderly subjects (over 60 years) according to WHO classification (≥ 20 blasts in bone marrow), who did not accept or were not eligible for chemotherapy (first line therapy)
• Subjects with chronic myeloid leukaemia in chronic or accelerated phase, resistant or intolerant to standard treatment, who have not achieved a complete haematological response, and are not candidates for allogeneic HSCT.
• Subjects with myeloproliferative disorders with no effective treatment options.
• Subjects with Philadelphia chromosome positive acute leukaemias including acute lymphoblastic leukaemia and blast phase chronic myeloid leukaemia, relapsing, resistant or intolerant to standard treatment with no effective treatment options.

You may not qualify if…

• Acute promyelocytic leukaemia.
• Ongoing uncontrolled bacterial, viral, fungal or atypical mycobacterial infection.
• Hyperleukocytosis with >50x10(9)/L leukaemic blasts.
• Chemotherapy, immunotherapy, biologic therapy or any experimental anti-cancer therapy within 28days prior to study Day1 and/or not having recovered from its toxicity.
• Extensive radiotherapy involving ≥30% of bone marrow (e.g. whole pelvis, half spine) within 6months prior to study Day1.
• Active CNS disease involvement.
• Any condition, including laboratory, medical history or pre-study assessment findings, that in the opinion of the Investigator, constitute a risk or contraindication for participation or that could interfere with the study objectives, conduct or evaluation of a drug to be taken orally.
• Clinically relevant cardiac abnormalities or clinically relevant abnormalities .
• Known infection with human immunodeficiency virus, active hepatitis B, or hepatitis C.
• Signs and symptoms suggestive of transmissible spongiform encephalopathy.
• Major surgery within 2weeks prior to study Day1.
• Haemoglobin <8g/dL at screening (can be transfused).
• Refractory to platelet transfusion (defined as increase of <20.109/L platelets 1hour after transfusion).
• Coexistent second malignancy or history of prior malignancy within previous 3years (excluding basal or squamous cell carcinoma of the skin, and in situ carcinoma of the cervix that has been treated curatively).

Where it is running

• CTRC at the UT Health Science Center at San Antonio — San Antonio, Texas, United States
• Haematologie UZ Gasthuisberg — Leuven, Belgium
• Mont-Godinne University Hospital (UCL) — Yvoir, Belgium
• Universitatsklinik Frankfurt — Frankfurt am Main, Germany
• Technische Universitat Munchen — München, Germany
• Medizinische Universitatsklinik — Ulm, Germany
• Policlinico Sant'Orsola Malpighi — Bologna, Italy
• Kantonsspital Basel — Basel, Switzerland
• Hospitaux Universitaires — Geneva, Switzerland
• Kantonsspital St Gallen — Sankt Gallen, Switzerland

Full record on ClinicalTrials.gov

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