Merck/Gilead Once-A-Day AIDS Pill Not Available in Most Places - AHF Urges Speed-Up of Registrations

LOS ANGELES--10 Sep--PRNewswire-AsiaNet/InfoQuest


The once-daily HIV treatment would greatly increase effectiveness for patients, but Gilead Sciences and Merck and Co. have failed to register it in countries where it is needed most

AIDS Healthcare Foundation (AHF) today called on Gilead Sciences and Merck to immediately register and distribute the three-in-one, once daily lifesaving HIV treatment, Atripla, in developing countries. When Atripla first received approval from the Food and Drug Administration (FDA) in July of 2006, advocates like AHF applauded the production of a single, once-a-day drug as a landmark

step in treating HIV. However, since its approval, little progress has been made in expanding the availability of the treatment in the developing world, where only 28% of those in need of treatment were able to access it as of December 2006. Efforts made by AHF to clarify what countries currently can purchase Atripla at the announced $613 per patient per year access price have gone unanswered.

"This treatment is a standard therapy in the United States. It is on the World Health Organization's Essential Medicines List, and is an antiretroviral drug regimen that could greatly benefit patients everywhere while reducing costs in the long term," said Michael Weinstein, AIDS Healthcare Foundation President. "The fact that Gilead and Merck appear to be unable or unwilling to

make it available in resource-poor countries is deeply troubling, and causing unnecessary suffering. Gilead and Merck should immediately begin making this treatment available to the rest of the world, or license it out to a generic drug manufacturer, such as Cipla, which already produces a generic version in India, that will. In the instances where the registration process has been initiated such as in the European Union, governments must also recognize their roles and streamline the necessary approval processes to facilitate quick distribution of these lifesaving drugs."

The key value of an all-in-one, one pill per day HIV treatment regimen is the reduced pill burden required for patients. Currently, the most widely used regimen for treatment naive patients consists of a combination of at least two pills taken twice per day, often required to be taken with food and during mid-day hours. Atripla, however, only requires a single pill to be taken once

daily without food before bed.

"As we have seen in many of our clinics, pill burden and side effects can be challenging for patients to become accustomed to, and they are among the primary reasons patients do not follow their treatment regimens," said Dr. Homayoon Khanlou, AIDS Healthcare Foundation's Chief of Medicine. "With a complete daily treatment regimen in one pill, the advantage goes much further

than simply fewer pills and fewer side effects. The ease of treatment results in improved adherence with more patients taking their medication as prescribed, which greatly increases the effectiveness of treatment. This also results in fewer patients developing resistance to the drugs, and from having to move on to more expensive second-line drugs."

AIDS Healthcare Foundation (AHF) is the nation's largest non-profit HIV/AIDS healthcare, research, prevention and education provider. AHF currently provides medical care and/or services to more than 61,000 individuals in 15 countries worldwide in the US, Africa, Latin America/Caribbean and Asia. Additional information is available at http://www.aidshealth.org .

If you have received this news release in error and do not wish to receive future advisories, or if they should be directed to someone else in your organization, please call (323) 860-5262. Alternatively, you may fax your updated information or your request for removal from our list to (323) 962-8513 or e-mail [email protected].

SOURCE: AIDS Healthcare Foundation

CONTACT: Ged Kenslea, Communications Director of AIDS Healthcare

Foundation, +1-323-860-5225, Mobile: +1-323-791-5526,

[email protected]/

Web site: http://www.aidshealth.org /

--Distributed by AsiaNet ( www.asianetnews.net )--


ข่าวGilead Sciences+o:healวันนี้

GILEAD LAUNCHES GLOBAL ALL4LIVER GRANT PROGRAM TO HELP ACHIEVE THE WORLD HEALTH ORGANIZATION'S GOAL OF VIRAL HEPATITIS ELIMINATION BY 2030

- Gilead expands the ALL4LIVER Grant, Providing Grant Funding to Organizations in Africa, South America, Asia and Oceania, Europe and North America - Themed 'Test. Link. Prioritize', the Grant Program will Target Projects Focusing on Viral Hepatitis Elimination by 2030 - Gilead Sciences, Inc. (Nasdaq: GILD) today announced the launch of the 2023 Gilead ALL4LIVER Grant, a grant program with the theme of 'Test. Link. Prioritize', designed to support innovative projects that drive testing, improve

Results are part of the first Asia Pacifi... PEOPLE LIVING WITH HIV AND INDIVIDUALS AT-RISK EXPERIENCED DISRUPTION TO HIV CARE IN THAILAND: SURVEY — Results are part of the first Asia Pacific-wide su...

Hetero Enters Into a Licensing Agreement With Gilead Sciences, Inc. for the Manufacturing and Distribution of "Remdesivir" in 127 Countries, Including India, for COVID-19

Hetero, one of India's leading generic pharmaceutical companies and the world's largest producer of anti-retroviral drugs,...

Hetero ลงนามในสัญญาอนุญาตให้ใช้สิทธิกับ Gilead Sciences เพื่อผลิตและจัดจำหน่ายยาต้านโควิด-19 “Remdesivir” ใน 127 ประเทศ รวมถึงอินเดีย

Hetero ผู้ผลิตยาสามัญชั้นแนวหน้าของอินเดียและผู้ผลิตยาต้านรีโทรไวรัสรายใหญ่ที่สุดของโลก ประกาศว่า ทางบริษัทได้ลงนามในสัญญาอนุญาตให้ใช้สิทธิกับ Gilead Sciences, Inc. ...

Cipla Enters Into a Licensing Agreement With Gilead to Expand Access to COVID-19 Treatment

Cipla Limited (BSE: 500087) (NSE: CIPLA EQ) (and hereafter referred to as "Cipla") today announced that it has signed a non-exclusive licensing agreement with Gilead Sciences, Inc. for the manufacturing and...

Cipla บรรลุข้อตกลงอนุญาตใช้สิทธิกับ Gilead มุ่งขยายการเข้าถึงการรักษาโรคโควิด-19

Cipla Limited (BSE: 500087) (NSE: CIPLA EQ) (และกล่าวถึงในที่นี้ว่า “Cipla”) ประกาศในวันนี้ว่า บริษัทได้ลงนามในข้อตกลงอนุญาตใช้สิทธิโดยไม่จำกัดแต่เพียงผู้เดียวกับ Gilead Sciences, Inc. เพื่อผลิต...

กว่าหมื่นรายชื่อเรียกร้องบริษัทยาหยุดผูกขาดตลาดขายยาไวรัสตับอักเสบซีเม็ดละสามหมื่น

คนไทยกว่าหมื่นคนร่วมลงชื่อผ่าน Change.org/StopGilead เรียกร้องบริษัทยากิลิแอด (Gilead Sciences, Inc.) ผู้คิดค้นและผลิตยาไวรัสตับอักเสบซีที่มีประสิทธิภาพสูงสุดในท้องตลาดขณะนี้ ให้หยุดผูกขาดตลาดและเลิกขายยาราคาเม็ดละ 3...

Janssen Announces Collaboration with Gilead to Develop PREZISTA(R)-based Single-tablet Regimen for the Treatment of People Living with HIV

Two Companies to also Collaborate on the Further Development of Complera(R), Marketed as Eviplera(R) in the European Union Janssen R&D Ireland (Janssen) announced...

Janssen Submits Marketing Authorisation Application to European Medicines Agency for a Fixed-Dose Combination Tablet of HIV-1 Medicine Darunavir with Cobicistat

Janssen-Cilag International NV (Janssen), today announced it has submitted a Marketing Authorisation Application to the European Medicines...

สรุปข่าวเอเชียเน็ทประจำวันจันทร์ที่ 10 กันยายน 2550

การรักษาโรคเอดส์ ลอสแองเจลิส: มูลนิธิดูแลสุขภาพผู้ป่วยเอดส์ (AHF) เรียกร้องให้บริษัท จีลีด ไซแอนเซส (Gilead Sciences) และ เมอร์ค (Merck) เร่งจดทะเบียนในทันที และจัดจำหน่ายยาอาตริพลา (Atripla) ซึ่งเป็นยารักษาโรคเอดส์แบบ 3 in 1 และรับประทานเพียงวันละ...