Research on New Treatment for Neglected Disease Published in The New England Journal of Medicine.Paromomycin IM Injection to Treat Visceral Leishmaniasis Advantageous for Safety, Efficacy, and Practicality SAN FRANCISCO & NEW DELHI, India -- The Institute for OneWorld Health The Institute for OneWorld Health is a 501(c)(3) nonprofit pharmaceutical company founded in 2000 to develop safe, effective, and affordable new medicines for people with infectious diseases in the developing countries. , a US-based non-profit pharmaceutical company, today announced that Phase 3 research related to its first approved drug product, Paromomycin IM Injection (Paromomycin), was published in the current issue of The New England Journal of Medicine The New England Journal of Medicine (New Engl J Med or NEJM) is an English-language peer-reviewed medical journal published by the Massachusetts Medical Society. It is one of the most popular and widely-read peer-reviewed general medical journals in the world. (NEJM NEJM New England Journal of Medicine ). This clinical trial shows that the medicine paromomycin is safe, effective, and well suited to curing visceral leishmaniasis (VL), the world's second most deadly parasitic disease after malaria. The Institute for OneWorld Health, working closely with the Indian Council for Medical Research (ICMR ICMR Indian Council of Medical Research ICMR Institute for Coastal and Marine Resources ICMR Interagency Committee on Medical Records ) sponsored the clinical trial in collaboration with the Special Programme for Research and Training in Tropical Diseases (TDR), a Geneva-based international organization sponsored by UNICEF UNICEF (y `nĭsĕf'), the United Nations Children's Fund, an affiliated agency of the United Nations. , UNDP UNDP United Nations Development ProgrammeUNDP Unión Nacional para la Democracia y el Progreso (National Union for Democracy and Progress) , the World Bank and the World Health Organization. The clinical trial was established with funding from the Bill & Melinda Gates Foundation. Gland Pharma Limited, the Hyderabad, India-based drug manufacturer, working with OneWorld Health and other collaborators, received regulatory approval from the Drug-Controller General - India (DCGI) for Paromomycin IM Injection as a treatment for VL on August 31, 2006. Gland Pharma has agreed to act as the global manufacturer of Paromomycin to ensure access to all those that need it, and at a markedly reduced cost -- currently, approximately $10 USD USD In currencies, this is the abbreviation for the U.S. Dollar. Notes: The currency market, also known as the Foreign Exchange market, is the largest financial market in the world, with a daily average volume of over US $1 trillion. per 21-day course of therapy. "The results of this study underscore the potential of Paromomycin to treat VL -- and save lives -- at very low cost and in safe and practical ways," said Dr. Ahvie Herskowitz, co-founder and chief medical officer of the Institute for OneWorld Health. "This research is essential to increasing access to new therapies for this neglected disease, also known as kala-azar and black fever." With approximately 500,000 new cases occurring annually worldwide, VL primarily afflicts the rural resource-poor populations in India, Nepal, Bangladesh, Sudan and Brazil, where affordable new therapies are needed. The print issue of the publication will be available in the June 21, 2007, issue of the NEJM. The article, "Injectable Paromomycin for Visceral Leishmaniasis in India," was authored by Shyam Sundar, M.D., T.K. Jha, M.D., Chandreshwar P. Thakur, M.D., Prabhat K. Sinha, M.D., and Sujit K. Bhattacharya, M.D., Principal Investigators in the Phase 3 clinical trial phase 3 clinical trial Phase 3 study. See Phase study. . The article is accessible online, and can be found at www.nejm.org under the "Current Issue" section of the Web site. The researchers conducted a randomized ran·dom·ize tr.v. ran·dom·ized, ran·dom·iz·ing, ran·dom·iz·es To make random in arrangement, especially in order to control the variables in an experiment. , controlled, phase 3 study comparing Paromomycin, an aminoglycoside aminoglycoside /ami·no·gly·co·side/ (-gli´ko-sid) any of a group of antibacterial antibiotics (e.g., streptomycin, gentamicin) derived from various species of Streptomyces , and amphotericin B, the present standard of care in Bihar, India. Paromomycin was shown to be noninferior to amphotericin B with a final cure rate of 94.6% vs. 98.8% for amphotericin. Paromomycin also had an acceptable safety profile, which included mild injection-site pain in 55% of patients and transient increases in liver function values in 6% of patients. The NEJM reports that Paromomycin may be advantageous because of the shorter duration of its administration (21 days versus 30 days for amphotericin B), its demonstrated safety and efficacy in pediatric patients (96%) and in patients who failed to be cured with other medicines (98%). The NEJM article concluded, "The healthcare delivery system in India is well suited to the intramuscular intramuscular /in·tra·mus·cu·lar/ (-mus´ku-ler) within the muscular substance. in·tra·mus·cu·lar adj. Abbr. IM Within a muscle. administration of Paromomycin under directly observed therapy directly observed therapy Therapeutics A strategy for ensuring Pt compliance with therapy, where a health care worker or designee watches the Pt swallow each dose of prescribed drugs. See Patient compliance. Cf Directed observation. , and the local manufacture of Paromomycin in India, potentially at a very low cost, makes this an approachable therapy in the setting of limited resources." Earlier this year, the World Health Organization (WHO) selected Paromomycin IM Injection for inclusion on its Model List for Essential Medicines. The WHO List of Essential Medicines provides a model for countries to select medicines addressing public health priorities according to quality, safety and efficacy standards. About Visceral Leishmaniasis VL is a systemic infection caused by various species of Leishmania Leishmania /Leish·ma·nia/ (lesh-ma´ne-ah) a genus of parasitic protozoa, including several species pathogenic for humans. In some classifications, organisms are placed in four complexes comprising species and subspecies: L. parasites. The infection is transmitted by sandflies and causes chronic fever, weight loss, splenomegaly splenomegaly /sple·no·meg·a·ly/ (-meg´ah-le) enlargement of the spleen. congestive splenomegaly Banti's disease; splenomegaly secondary to portal hypertension. , hepatomegaly hepatomegaly /hep·a·to·meg·a·ly/ (hep?ah-to-meg´ah-le) enlargement of the liver. hep·a·to·meg·a·ly n. The abnormal enlargement of the liver. Also called megalohepatia. and anemia. Left untreated, VL is nearly always fatal. VL currently occurs in 62 countries, primarily in the developing world. Of the approximately 500,000 new cases of VL occurring annually, 90% are found in just five countries: India, Bangladesh, Nepal, Sudan and Brazil. South Asia carries 70% of all estimated new VL cases per year worldwide, with India alone carrying 50% of all new cases. The most affected state in India is Bihar, but VL is also endemic in the states of Jharkand, West Bengal, and Uttar Pradesh. About Paromomycin Phase 3 Clinical Trial The approval of Paromomycin IM Injection in India is based on data from a large Phase 3 multi-center, randomized, controlled study of 667 adult and pediatric patients conducted in Bihar State, India over a 17-month period from June 2003 until November 2004. Paromomycin was shown to cure 94.6% of patients with VL, with an acceptable side effect profile. The most common adverse reaction among patients treated with Paromomycin was mild pain at the injection site. About Paromomycin IM Injection An off-patent aminoglycoside antibiotic, paromomycin is an established drug with an extensive and well-characterized safety profile. Paromomycin IM Injection is now available from Gland Pharmaceuticals (Hyderabad, India) for the first time as a new treatment of VL in India as a once-a-day injection for 21 days. The cost of Paromomycin IM Injection is significantly lower than other currently approved VL therapies. About the Institute for OneWorld Health The Institute for OneWorld Health, the first US non-profit pharmaceutical company, develops safe, effective and affordable medicines for people with neglected diseases of the developing world. The Institute for OneWorld Health, headquartered in San Francisco, California “San Francisco” redirects here. For other uses, see San Francisco (disambiguation). The City and County of San Francisco (EN IPA: [sænfrənˈsɪskoʊ] , USA, is a tax-exempt 501(c)(3) US corporation. (http://www.oneworldhealth.org/). Media resources are available at http://www.oneworldhealth.org/media/index.php/. |
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