10-QPeriod: Q1 FY2005

Merck & Co., Inc. Quarterly Report for Q1 Ended Mar 31, 2005

Filed April 26, 2005For Securities:MRK

Summary

Schering-Plough Corporation reported a net income of $127 million for the first quarter of 2005, a significant turnaround from a net loss of $73 million in the same period of the prior year. This improvement was primarily driven by a substantial increase in equity income from its cholesterol joint venture with Merck, which contributed $220 million, including a $14 million milestone payment. Consolidated net sales also rose by 21% to $2.4 billion, fueled by growth in prescription pharmaceuticals, particularly from new agreements with Bayer for AVELOX and CIPRO, and a positive foreign exchange impact. Despite the reported net income, the company's financial situation remains complex. Cash flow from operations was $200 million, but the company repaid approximately $1.2 billion in commercial paper borrowings. The company's strategy focuses on increasing profitability from its cholesterol franchise (VYTORIN and ZETIA) and controlling expenses. However, management notes that maintaining historical investment levels in marketing and research is not sustainable without significant profit and cash flow growth, and that strategic alternatives might need to be evaluated if this cannot be achieved. Significant ongoing legal and regulatory matters, including investigations into sales and marketing practices and the resolution of a consent decree with the FDA, continue to pose financial and commercial risks.

Key Highlights

  • 1Schering-Plough returned to profitability, reporting a net income of $127 million for Q1 2005, compared to a net loss of $73 million in Q1 2004.
  • 2Consolidated net sales increased by 21% year-over-year to $2.4 billion, driven by prescription pharmaceuticals, including contributions from the Bayer agreement for AVELOX and CIPRO.
  • 3Equity income from the cholesterol joint venture with Merck significantly boosted earnings, totaling $220 million, up from $78 million in the prior year, partly due to a $14 million milestone payment.
  • 4The company repaid $1.2 billion in commercial paper borrowings, while net cash provided by operating activities was $200 million.
  • 5Ongoing legal and regulatory challenges, including investigations and an FDA consent decree, continue to present significant financial and commercial risks.
  • 6Schering-Plough is implementing a multi-year 'Action Agenda' to stabilize, repair, and turn around the business, focusing on the cholesterol franchise and cost control.

Frequently Asked Questions

The primary driver is a significant increase in equity income from the cholesterol joint venture with Merck & Co., Inc. This income rose to $220 million in Q1 2005 from $78 million in Q1 2004, bolstered by a $14 million milestone payment and a larger share of profits from the successful ZETIA and VYTORIN products.

The company repaid approximately $1.2 billion of commercial paper borrowings in the quarter. While operating cash flow was positive at $200 million, management indicates that maintaining historical investment levels in marketing and research is not sustainable without significant profit and cash flow growth. They also noted that the company is relying on repatriated foreign earnings and a credit facility to manage U.S. operations' negative cash flow in the intermediate term.

Key risks include ongoing investigations into sales and marketing practices (particularly the Massachusetts investigation which carries significant financial and commercial risks), compliance with the FDA consent decree for manufacturing facilities, potential for significant legal liabilities, increased competition and pricing pressure in pharmaceutical markets, and the challenge of generating sufficient profits and cash flow to sustain R&D and marketing investments.

The company is actively working to fulfill the requirements of the consent decree, which involves comprehensive work plans and revalidation programs for manufacturing facilities. While progress has been made, the company acknowledges the risk of missing deadlines, which could lead to payments to the FDA and potentially impact product approvals and production. This has resulted in increased costs and reduced output at affected facilities.