RHONE-POULENC DRUG STRATEGY INCLUDES "EVENTUAL" U.S. EXPANSION

RHONE-POULENC DRUG STRATEGY INCLUDES "EVENTUAL" U.S. EXPANSION, the French chemical/diversified company reported in a recent filing with the Securities & Exchange Commission covering a planned public offering. "Eventual expansion into key geographical markets such as the U.S. and Japan is . . . targeted, but the cost of entry into these markets is relatively high," the registration statement notes. Rhone-Poulenc observed that it has "historically adopted a policy of licensing, rather than direct sales, of its ethical pharmaceuticals" in the U.S. The company's major product lines are distributed in the U.S. by Searle (Flagyl), SmithKline (prochlorperazine) and American Home Products (Orudis, Sectral and Phenergan). These licensing agreements combined with the recent acquisitions of two bulk pharmaceutical businesses in the U.S., U.S. Ethicals and Purification Engineering, Rhone-Poulenc noted, "give the company a small foothold in the U.S. market." In addition, the French firm already has its own research and registration facility in Mon-mouth Junction, N.J. for "future products." However, before expansion into new markets, Rhone-Poulenc reported that its first priority in the health care area is to "supplement internal growth with selective acquisitions" in geographic therapeutic areas where the company has already established a strong position. Geographically, Rhone-Poulenc cited Europe, Africa and South America. Drug markets with potential for expansion, Rhone-Poulenc said, are infectious diseases, cardiovasculars, anti-rheumatics, vaccines, analgesic bulk chemicals and vitamins. In addition, Rhone-Poulenc said it plans to invest in research to develop new chemical entities and in OTC pharmaceuticals. In 1986, the nonsteroidal anti-inflammatory Orudis (ketaprofen) surpassed Flagyl (metronidazole) as Rhone-Poulenc's topselling Rx product worldwide. The previous year, Flagyl had accounted for 19% of the company's over $1.2 bil. in pharmaceutical sales, or approximately $240 mil. Rhone-Poulenc's other leading Rx product areas in 1985 were the cardiovascular agents, Sermion (nicergoline) and Sectral (acebutolol), which together had worldwide sales of roughly $225 mil., serums and vaccines, with sales of approximately $150 mil., psychotropics, led by Stemetil (prochlorperazine), with sales of about $135 mil., and the anti-infectious agents, Josacine (josamycine) and Rovamycine (spiramycine), with combined 1985 sales of roughly $75 mil. Reflecting Rhone-Poulenc's aggressive acquisition program in recent years, nearly one-third of the company's pharmaceutical business is now being derived from businesses acquired since 1983. That year Rhone-Poulenc acquired the French drug firm Pharmuka, which contributed sales of approximately $120 mil. in 1985. In 1986, Rhone-Poulenc accelerated its acquisition program with four international acquisitions that, combined, generated sales of approximately $280 mil. Rhone-Poulenc's largest drug acquisition in 1986, by far, was the West German firm A. Natterman & Cie GmbH with annual sales over $200 mil. Rhone-Poulenc also made three other drug acquisitions with sales in the $20-$30 mil. range, including Upjohn Brazil, the Italian firm Roger Bellon Schoum S.p.a., and Gerot, based in Austria.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Archive

Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval

 

Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.

Final Chance To Have Your Say: Take Our Reader Survey This Week

 
• By 

This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Shape Our Content: Take The Reader Survey

 
• By 

We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in coverage topics, article format, or the method in which you access the Pink Sheet – or if you love it how it is – now is the time to have your voice heard.

Brazil Pilots Digital Drug Pack Inserts

 

A new pilot aims to take Brazil closer to ‘digital transformation.’

More from Pink Sheet

EMA Explores Supporting Drug Development For High Unmet Need Disorder Scleroderma

 

While treatments for scleroderma are in development, none are approved for the condition that is associated with high morbidity and mortality. The European Medicines Agency says guidance on how to design development programs for the disorder is needed.

EMA Nod For First MASH Drug Rezdiffra, Cell Therapy Zemcelpro And 11 Others

 

Madrigal Pharmaceuticals’ Rezdiffra is on track to become the first medicine approved in the EU for non-cirrhotic metabolic dysfunction-associated steatohepatitis after the European Medicines Agency recommended that it be granted conditional marketing authorization.

BIO Notebook: Policy Uncertainty Constraining Dealmaking

 

Highlights from Day Four of the BIO International Convention include policy concerns helping constrain dealmaking, Novartis discussing its approach to partnering, and Generate looking for funding to move into Phase III.