ZD6126
ZD6126 is a vasculature-disrupting agent that was developed by AstraZeneca for the treatment of cancer. It is a tubulin-binding agent that destabilizes tumor vasculature, leading to extensive tumor cell death.
Mechanism of Action[edit | edit source]
ZD6126 works by binding to the colchicine binding site of beta-tubulin, which leads to the destabilization of microtubules. This destabilization results in the disruption of the newly formed blood vessels within tumors, causing extensive tumor cell death.
Clinical Trials[edit | edit source]
ZD6126 has undergone Phase I and II clinical trials for the treatment of various types of cancer. However, the development of the drug was discontinued due to adverse side effects.
Side Effects[edit | edit source]
The most common side effects of ZD6126 include nausea, vomiting, and fatigue. Serious side effects can include neutropenia, thrombocytopenia, and anemia.
See Also[edit | edit source]
References[edit | edit source]
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