(BW) Clinical Data For Sequus Pharmaceuticals' AMPHOTEC Product Indicate Safety And Efficacy In Treatment Of Refractory Patients With Systemic Candida Fungal Infections

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(BW) Clinical Data For Sequus Pharmaceuticals' AMPHOTEC Product Indicate Safety And Efficacy In Treatment Of Refractory Patients With Systemic Candida Fungal Infections

BUSINESS WIRE - 44 Montgomery St, 39th Floor, San Francisco, CA 94104; Tel: (415) 986-4422; FAX: (415) 788-5335 -


NEW ORLEANS--(BUSINESS WIRE)--Sept. 19, 1996--Data from five open label trials of AMPHOTEC(TM) in the treatment of invasive fungal infection, reviewed today at the 34th Annual Meeting of the Infectious Diseases Society of America by Dr. Gary Noskin of Northwestern Memorial Hospital and Northwestern University Medical School, indicate that AMPHOTEC is safe and effective in the treatment of seriously ill patients with Candida blood stream infection (candidemia).

AMPHOTEC, also known as amphotericin B colloidal dispersion or ABCD is being developed by SEQUUS Pharmaceuticals, Inc. (Nasdaq: SEQU) to treat progressive and potentially fatal systemic fungal infections. Data derived from this retrospective analysis need to be confirmed in randomized, prospective comparative trials.

A total of 149 patients with blood cultures positive for Candida were treated with AMPHOTEC during a course of five clinical trials. All patients had either failed standard amphotericin B therapy or had kidney toxicity due to amphotericin B or other causes which precluded therapy with amphotericin B and, thus, were considered refractory to standard therapy. Of these patients, a total of 72 were evaluable for efficacy (defined as having received seven doses of AMPHOTEC within the first ten days of entering the trial and no concurrent systemic antifungal therapy).

Nineteen of the 72 evaluable patients had disseminated Candidal infection, while 53 had candidemia only. The response rate in those with candidemia only was 69.8 percent (37/53), including 35 complete responses and two partial responses, while the response rate in patients with dissemination of the Candida infection was 26.3 percent (5/19), including three complete and one partial responses. Based on measurement of serum creatinine levels, there was no evidence of nephrotoxicity related to the study drug.

AMPHOTEC, marketed as AMPHOCIL(TM) outside the U.S., is approved for use in 16 countries. A New Drug Application for this product is under review by the U.S. Food and Drug Administration.

Established in 1981 and headquartered in Menlo Park, Calif. (with offices in London, England), SEQUUS is developing proprietary pharmaceutical products for the treatment of cancer and other life-threatening diseases.

CONTACT: SEQUUS Pharmaceuticals, Inc., Menlo Park I. Craig Henderson, M.D., Chairman and CEO Scott Minick, President and COO Donald J. Stewart, VP, Finance and Treasurer 415/323-9011 or Ogilvy Adams & Rinehart (Media Inquiries) Timothy Sipols, 212/880-5251 or Burns McClellan (Investor Inquiries) John Nugent, 212/505-1919


Keywords: CANDIDA; CLINICAL TRIAL

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