Volitinib

From WikiMD's Wellness Encyclopedia

Volitinib (development code HMPL-504) is a small molecule inhibitor specifically designed to target the c-Met receptor tyrosine kinase. It is primarily researched for its potential use in the treatment of various types of cancer, including gastric cancer and non-small cell lung cancer (NSCLC) that exhibit aberrant c-Met activity.

Mechanism of Action[edit | edit source]

Volitinib acts by selectively inhibiting the activity of the c-Met tyrosine kinase, which is a critical component in the Hepatocyte Growth Factor Receptor (HGFR) signaling pathway. This pathway is known to play a significant role in cellular growth, migration, and angiogenesis. Abnormal activation of c-Met has been implicated in the development and progression of several cancers by promoting oncogenesis, angiogenesis, and cancer metastasis. By inhibiting this pathway, volitinib aims to reduce tumor growth and spread.

Clinical Development[edit | edit source]

The clinical development of volitinib has included several phases of clinical trials primarily focusing on its efficacy and safety in patients with cancers that have high levels of c-Met expression. Early-phase clinical trials have explored its pharmacokinetics, pharmacodynamics, and preliminary efficacy.

Phase I Trials[edit | edit source]

Initial Phase I trials aimed to determine the optimal dosing strategy, assess safety profiles, and identify potential side effects in a small group of patients. These studies also provided initial data on the drug's anti-tumor activity.

Phase II Trials[edit | edit source]

Following promising Phase I results, volitinib entered Phase II trials, which focused more on its efficacy in larger groups of patients with specific types of c-Met-dependent tumors. These studies are crucial for determining the drug's effectiveness in a more targeted patient population and further assessing its safety.

Regulatory Status[edit | edit source]

As of the last update, volitinib is still under clinical investigation and has not yet received approval from regulatory bodies such as the Food and Drug Administration (FDA) or the European Medicines Agency (EMA). The outcomes of ongoing clinical trials will determine its future in the pharmaceutical market.

Potential Impact and Future Directions[edit | edit source]

If approved, volitinib could provide a new therapeutic option for patients with c-Met-driven cancers, potentially improving survival rates and quality of life. Future research may also explore its use in combination with other therapeutic agents, which could enhance its efficacy and broaden its applicability in oncology.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD