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Sponsored by: |
AstraZeneca |
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Information provided by: | AstraZeneca |
ClinicalTrials.gov Identifier: | NCT00088790 |
Purpose of this study is to assess the safety and tolerability of AZD5438 given orally to patients with advanced solid malignancies A review of the emerging clinical tolerability and exposure data from this study in conjunction with preclinical and the available clinical pharmacodynamic data relating to AZD5438, led to a decision by AstraZeneca that the development of AZD5438 as a potential anti-cancer agent would be discontinued.
Condition | Intervention | Phase |
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Neoplasms |
Drug: AZD5438 |
Phase I |
Study Type: | Interventional |
Study Design: | Treatment |
Official Title: | Phase I Study to Assess the Safety and Tolerability of AZD5438 in Patients With Advanced Solid Malignancies |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | D0110C00005 |
Study First Received: | August 4, 2004 |
Last Updated: | April 14, 2008 |
ClinicalTrials.gov Identifier: | NCT00088790 |
Health Authority: | United States: Food and Drug Administration |
advanced, solid, malignancies |
Neoplasms |