IntelenceTreatment for HIV Infection
Update: Intelence Now FDA Approved - January 18, 2008
New Drug Application for Investigational HIV Treatment TMC125 Submitted to U.S. Food and Drug Administration
YARDLEY, Pa., July 18, 2007 /PRNewswire/ -- Tibotec Pharmaceuticals Ltd. today announced the submission of a New Drug Application to the U.S. Food and Drug Administration (FDA) for TMC125 (etravirine), an investigational non- nucleoside reverse transcriptase inhibitor (NNRTI), being studied for use with other antiretroviral (ARV) agents as a treatment for people infected with HIV- 1.
The submission is based on the 24-week efficacy and safety results of two Phase III randomized, placebo-controlled studies, known as DUET-1 and DUET-2, which studied the use of TMC125 in combination with other antiretroviral agents in adult treatment-experienced HIV-1 patients with documented resistance to NNRTIs and protease inhibitors (PIs). Data from these studies were published in the July 7, 2007 issue of The Lancet and will be shown at a late-breaker presentation at the 2007 International AIDS Society (IAS) conference in Australia on July 25th.
TMC125 is the first NNRTI to show antiviral activity in patients with documented NNRTI resistance. Tibotec has received fast track designation for TMC125 from the FDA. Under fast track designation in the FDA Modernization Act of 1997, FDA may expedite the review of a drug if it is intended for the treatment of a serious or life-threatening condition, and demonstrates the potential to address an unmet medical need for such a condition.
The expanded access program (EAP) for TMC125 is now open in a number of European countries, Canada and the United States. TMC125 is available to HIV-1 infected adults, at least 18 years old, who have limited treatment options either due to virological failure or intolerance to multiple ARV regimens. Patients must be three-class experienced, having received licensed treatment from each of the three major oral classes of anti-HIV drugs (NRTIs, NNRTIs, and PIs), unable to use currently approved NNRTIs due to resistance and/or intolerance and have received at least two PI-based regimens.
Pending US regulatory approval, Tibotec Therapeutics, a division of Ortho Biotech Products, L.P., will commercialize the product in the U.S. The trade name for the marketed product has not yet been determined. Regulatory submissions for TMC125 in other countries are expected in the coming months.
About Tibotec Therapeutics
Tibotec Therapeutics, a division of Ortho Biotech Products, L.P., headquartered in Bridgewater, N.J., is dedicated to delivering innovative virology therapeutics that help healthcare professionals address serious unmet needs in people living with HIV.
About Tibotec Pharmaceuticals Ltd.
Tibotec Pharmaceuticals Ltd., based in Cork, Ireland, is a pharmaceutical research and development company. The Company's main research and development facilities are in Mechelen, Belgium with offices in Yardley, PA. Tibotec is dedicated to the discovery and development of innovative HIV/AIDS drugs and anti-infectives for diseases of high unmet medical need.
Ortho Biotech Products, L.P. and Tibotec Pharmaceuticals Ltd. are subsidiaries of Johnson & Johnson.
(This press release contains "forward-looking statements" as defined in the Private Securities Litigation Reform Act of 1995. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could vary materially from the Company's expectations and projections. Risks and uncertainties include general industry conditions and competition; economic conditions, such as interest rate and currency exchange rate fluctuations; technological advances and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approvals; domestic and foreign health care reforms and governmental laws and regulations; and trends toward health care cost containment. A further list and description of these risks, uncertainties and other factors can be found in Exhibit 99 of Johnson & Johnson's Annual Report on Form 10-K for the fiscal year ended December 31, 2006. Copies of this Form 10-K, as well as subsequent filings, are available online at www.sec.gov, www.jnj.com or on request from the Company. The Company does not undertake to update any forward-looking statements as a result of new information or future events or developments.)
CONTACT: Media, Pamela Van Houten, +1-908-541-4137, Mobile,+1-908-295-7367, or Investors, Louise Mehrotra, +1-732-524-6491, or StanPanasewicz, +1-732-524-2524, or Lesley Fishman, +1-732-524-3922, all ofTibotec Pharmaceuticals Ltd.
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Posted: July 2007
- FDA Approves Intelence (etravirine) Tablets for Treatment-Experienced Pediatric Patients with HIV-1, Following Priority Review - March 27, 2012
- FDA Approves New Dosage Strength for Intelence - January 3, 2011
- U.S. Food And Drug Administration (FDA) Grants Traditional Approval for Intelence (etravirine) - December 2, 2009
- FDA Approves Intelence (etravirine) for HIV Combination Therapy - January 22, 2008
- FDA Accepts New Drug Application for Priority Review of Investigational HIV Treatment TMC125 - September 20, 2007