Polycap

From WikiMD's Wellness Encyclopedia

Polycap is a groundbreaking fixed dose combination (FDC) polypill, developed by Cadila Pharmaceuticals Limited, an esteemed pharmaceutical company based in Ahmedabad, India. This unique pill integrates moderate quantities of five distinct medications, targeting the prevention and reduction of heart attacks and strokes.

Composition and Mechanism[edit | edit source]

Polycap is meticulously designed to combine the following components:

  • Three blood pressure-regulating drugs.
  • A cholesterol reducer.
  • Aspirin.

Significantly, a 2009 study illuminated the potential of this combination, revealing a 50% reduction in the risk of heart attacks and strokes, compared to individuals who consumed each component separately. Impressively, there was no escalation in adverse effects[1].

The Concept of Fixed Dose Combinations (FDCs)[edit | edit source]

The idea of FDCs like Polycap has burgeoned in popularity, particularly with the appeal of minimizing the "pill burden" many patients experience. However, there's a double-edged sword: while FDCs might alleviate the mental stress of consuming multiple pills, they might not cater optimally to individual patient needs, potentially giving them superfluous or inadequate drug components.

Initially, Wald and Law postulated a six-drug concoction to be administered to patients over the age of 55 with increased risk of cardiovascular disease events. This would encompass:

Notably, after rigorous scrutiny showing no enhancement in patient outcomes with folic acid, it was consequently excluded from the Polycap by Cadila Pharmaceuticals.

As of now, "Polycap" amalgamates:

  • 100mg of aspirin.
  • 20mg of simvastatin (a cholesterol-reducing statin equivalent to Zocor).
  • Lower doses of blood pressure medications: atenolol (50mg), ramipril (5mg), and thiazide (12.5mg).

This multifaceted pill retains a compact size, ensuring ease of consumption[1].

The Indian Polycap Study (TIPS)[edit | edit source]

Cadila Pharmaceuticals Limited sponsored a pivotal study titled "The Indian Polycap Study (TIPS)". Coordinated by JP Parswani and Dr. Arun Maseeh, this study was meticulously helmed by Dr. Salim Yusuf from McMaster University, Hamilton, Ontario, and Dr. Prem Pais from St. John's Medical College, Bangalore, India.

This double-blind, controlled study delved into the effects of Polycap on 2,000 participants (average age 54). All participants exhibited at least one cardiovascular risk factor, such as diabetes, hypercholesterolemia, hypertension, obesity, or smoking[1].

During a 12-week period:

  • 400 participants consumed Polycap.
  • The rest were classified into eight groups, consuming either individual components or a combination thereof[1].

Those administered Polycap experienced a six to seven-point decrease in both systolic and diastolic blood pressure levels, thus hinting at a considerable reduction in heart disease and stroke risks[1].

Polycap PK Study[edit | edit source]

Conducted by Dr. Bhaswat Chakraborty and his team, the Polycap PK study confirmed the efficacy of Polycap in reducing multiple cardiovascular risks, along with ensuring the bioavailability of each of its components and nullifying potential drug-drug interactions[2].

Conclusion[edit | edit source]

Polycap signifies a revolutionary step in cardiovascular medication. While still necessitating comprehensive and global acceptance and distribution, it embodies the potential to reshape how cardiovascular risks are managed, especially in regions where pill burden is a pertinent concern.

See Also[edit | edit source]

External links[edit | edit source]

Polycap Resources
Wikipedia
  1. 1.0 1.1 1.2 1.3 1.4 Marchione, Marilynn via Associated Press. "Study says one combo pill does work of five", The Record (Bergen County), March 31, 2009. Accessed March 31, 2009.
  2. Preservation of Bioavailability of Ingredients and Lack of Drug-drug Interactions in a Novel Five Ingredient Polypill (PolycapTM) in a Five Arm Phase-I Crossover Trial in Healthy Volunteers, by Anil Patel, et al, Am. J. Cardiovasc. Drugs, 10: 95-103.
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