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FP021 is a small molecule drug candidate described as a cyclooxygenase-2 (COX-2) inhibitor. Its mechanism of action involves selective inhibition of the COX-2 enzyme, which plays a key role in the inflammatory process by catalyzing the conversion of arachidonic acid to prostaglandins. By inhibiting COX-2, FP021 is expected to reduce inflammation and pain. The primary target for this compound is COX-2, and it falls within the class of nonsteroidal anti-inflammatory drugs (NSAIDs), specifically as a COX-2 selective inhibitor[1]. No additional information about its developer, manufacturer, or clinical development status was found in available sources.
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