Drug therapy
development

Our therapeutics

Avenzoar specializes in developing small molecule therapeutics for cancer. Our lead drug, AP-001 (Metavert™), is a dual inhibitor small molecule designed to prevent cancer growth and metastasis. AP-001 has the potential to revolutionize cancer therapy.

Pre-clinical results | Trials

AP-001 is an innovative anti-cancer drug that targets two pro-cancer pathways simultaneously. Pre-clinical results show significant prevention of pancreatic cancer growth and metastasis with no significant toxicity. Clinical trials for pancreatic cancer patients are set to begin in 2025, with potential trials for ovarian and metastatic liver cancer to follow.

Pancreatic Cancer

Survival rates for pancreatic cancer are notably low, with only 12% of patients surviving beyond five years post-diagnosis, largely due  to late-stage diagnoses. Surgical removal of tumors is feasible in less than 20% of cases.

Current treatments primarily involve chemotherapy and radiation therapy, aiming to control the disease and improve patient quality of life.

12th

Most Prevalent
globally

495k

New Cases
Annually

466k

Deaths
Annually

64k

Diagnosed
Annually

12k

Five-year survival
Rate

Ovarian
Cancer

Source: World Ovarian Cancer Coalition

Five-year ovarian cancer survival rates vary between countries. For example, in more developed countries, current rates range from 36% to 46%. However, in some countries, the figure is much lower.

The five-year survival rate is 51%, falling well below that for other cancers. The first-line treatment for ovarian cancer typically includes surgery, followed by chemotherapy with platinum-based agents and a taxane.

8th

Most Prevalent
globally

324k

New Cases
Annually

207k

Deaths
Annually

19k

Diagnosed
Annually

51%

Five-year survival
Rate

Driving impact Together

Clinical Development

Our rigorous clinical development program is designed to meet the highest standards of regulatory scrutiny.

Regulatory Information

Avenzoar Pharmaceuticals is working closely with regulatory bodies, including the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA), to ensure that AP-001 meets all regulatory requirements for approval.

Events/Press

New drugs capable of targeting more than one oncogenic pathway may be one way to improve patient outcomes. This study characterizes the effectiveness of Metavert a first-in-class dual inhibitor of GSK3-β and histone deacetylase in treating PDAC

Metavert Synergises
Collaboration Opportunities

We are actively seeking collaboration opportunities with major pharmaceutical companies to bring AP-001 to patients. Engaging with industry leaders will enable us to leverage their manufacturing, distribution, and training capabilities to ensure that AP-001 reaches the pancreatic cancer patients who need it most.