Thursday, May 21, 2015

Helping doctors predict what's next for patients diagnosed with Hepatitis C

Helping doctors predict what's next for patients diagnosed with Hepatitis C

Patient risk model can help target costly HCV treatment to those with most urgent need

UNIVERSITY OF MICHIGAN HEALTH SYSTEM

ANN ARBOR, Mich. -- A team of researchers at the University of Michigan Health System has developed a risk prediction model that helps identify which hepatitis C patients have the most urgent need for new anti-viral drugs.

Rallying baby boomers to be screened for hepatitis C took off as effective treatments emerged to wipe out the liver-damaging virus. But high costs that can rise to more than $80,000 for a round of treatment have complicated the promise of providing curative treatment for the estimated 3.2 million people in the United States with hepatitis C.

For most patients, the disease will remain stable without treatment, perhaps for years and years, while one-third will have high risk of complications and need immediate care to prevent the virus from causing further liver damage, according to the U-M research.

The model, described in the June issue of Hepatology, uses routine lab values and machine-learning methods to help doctors predict the health outlook of patients diagnosed with hepatitis C.

"Offering immediate treatment to patients identified as high risk for poor health outcomes would allow these patients to benefit from highly effective treatments as other patients continue to be monitored and their risk assessment updated at each clinic visit," says lead study author Monica Konerman, M.D., MSc., a fellow in gastroenterology at the University of Michigan Health System.

Using a dataset from a previous National Institutes of Health study the Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C) trial, the U-M team used clinical data such as age, body mass index and virus type and routine lab measurements to estimate patients' risk of progression of liver disease.

The strength of the new model includes incorporation of many more lab values than most traditional models can handle. Plus, machine learning methods help analyze how lab values change over time, including the slope and acceleration of lab values such as platelet count, hepatic panel and AST to platelet ratio index (APRI), lab markers of liver injury and liver health.

Among the patients predicted as low-risk, only 6 percent will have cirrhosis (liver scarring) complications in the next year, compared to 56 percent in the high-risk group, according to the U-M study model.

"Ideally we would treat all patients. Until logistic and financial barriers are solved, clinicians and policy makers are faced with trying to target these therapies to patients with the most urgent need," Konerman says. "The model allows us to identify these patients with greater accuracy."

The risk prediction tool can be added to an existing electronic medical record as a health care decision guide for doctors. It can establish how often patients come in for doctor visits or and have monitoring tests.

The groundwork is being laid to make care accessible and affordable, including drug cost discounts for certain health care programs, and increased competition among drug companies that could potentially drive down prices.

Additional authors: Senior author Akbar K. Waljee, M.D., Anna S.F. Lok, M.D., Peter D.R. Higgins, M.D., Yiwei Zhang, of the University of Michigan Division of Gastroenterology and Ji Zhu, Ph.D., professor of statistics at the U-M College of Literature Science and Arts.

Reference: "Improvement of predictive models of risk of disease progression in chronic hepatitis by incorporating longitudinal data," Hepatology, official journal of the American Association for the Study of Liver Disease, Vol. 61, Issue No. 6, June 2015.

Funding: Researchers were supported by the National Institutes of Health and a Veterans Health Services Research and Development career development award.

Learn more about the Hepatology Program at the University of Michigan.

About U-M's Division of Gastroenterology: The U-M is one of the largest gastroenterology practices in the country and is a leader in the prevention, diagnosis, and treatment of diseases of the gastrointestinal tract and liver. Our 50-plus physicians are experts in the diagnosis and treatment of all diseases of the gastrointestinal system, from simple to complex, including those of the esophagus, stomach, small intestine, colon, rectum, liver, gallbladder, pancreas and biliary tract.

Wednesday, May 20, 2015

FDA Okays Hep-C Investigational Combo for Post-Transplant Patients

Press Release
Bristol-Myers Squibb Receives Amended U.S. FDA Breakthrough Therapy Designation for Investigational Daclatasvir-based Hepatitis C Regimen
Breakthrough Designation for daclatasvir and sofosbuvir combination is supported by the recently presented ALLY-1 trial in patients with advanced cirrhosis or recurrent hepatitis C (HCV) after liver transplant
FDA Designation signifies that high unmet need still exists among these patient populations despite other available therapies
This Designation is separate from the FDA’s ongoing NDA review of a daclatasvir-sofosbuvir regimen for the treatment of patients with genotype 3 HCV

FDA Okays Hep-C Investigational Combo for Post-Transplant Patients
May 20, 2015 | Gale Scott

Based on favorable results from the ALLY-1 trial, the US Food and Drug Administration (FDA) has amended its breakthrough therapy designation for a hepatitis-C drug combo.

The change means that daclatasvir (Daklinza/ Bristol-Myers Squibb) and sofosbuvir (Sovaldi/Gilead ) may now be given to patients who have hepatitis C infections with either advanced cirrhosis or infections that have come back after patients received a liver transplant.

The trial results were presented last month at the 2015 International Liver Congress in Vienna, Austria.

The trial found the treatment worked for patients with hepatitis C viral genotype 1, a common type in the US.

These patients had advanced liver disease, classified as Child-Pugh class B or class C and are difficult to cure.

Discussing the trial results in an interview in Vienna last month, investigator Fred Poordad, MD, of the University of Texas Health Science Center in San Antonio, TX, said eradicating the virus is difficult, even after transplantation. The virus continues to live in the patient’s blood and most patients who get a transplant who were infected before the surgery will develop cirrhosis within 5 years, Poordad said.

The FDA first granted a breakthrough therapy designation for the drug combo in 2013. It is given for 12 weeks, once daily, in combination with ribavirin.

The ALLY-1 study was the third to be reported as part of the Bristol-Myers Squibb ALLY research program. Two others, ALLY-2 and ALLY-3, were presented at the 2015 Conference for Retroviral and Opportunistic Infections and the 2014 American Association for the Study of Liver Diseases' The Liver Meeting, respectively. Additionally, the European Association for the Study of the Liver included the ALLY regimen in HCV treatment guidelines it issued last month.

The FDA is currently reviewing a new drug application for the use of daclatasvir and sofosbuvir to treat patients with HCV genotype 3. Daclatasvir was approved in Europe in August 2014 for use in combination with other drugs across genotypes 1, 2, 3 and 4 for the treatment of HCV infection in adults. Beyond Europe, it is approved in Japan, as well as multiple countries in Latin and South America, the Middle East and Asia Pacific.

Bristol-Myers pointed out that this is separate from the FDA's consideration of the combo drug for treatment of patients with genotype 3 hep C. The combo drug has been approved in Japan and in some countries in Europe but has yet to get an FDA nod so that it can find its place in a market that Gilead had to itself for a year before AbbVie got its combo drug approved late last year.

AbbVie is just getting started in the market, but ...


Dasabuvir in hepatitis C: Indication of added benefit in certain patients

Dasabuvir in hepatitis C: Indication of added benefit in certain patients

The drug dasabuvir (trade name Exviera) has been available since January 2015 for the treatment of adults with chronic hepatitis C infection. The German Institute for Quality and Efficiency in Health Care (IQWiG) examined in a dossier assessment whether this drug offers an added benefit over the appropriate comparator therapy.

According to the findings, there are indications of an added benefit in patients who have not yet developed cirrhosis of the liver and who are infected with the hepatitis C virus (HCV) genotype 1a. In case of genotype 1b, this only applies to treatment-naive, but not to treatment-experienced patients. The extent of added benefit is non-quantifiable, however. No added benefit can be derived from the dossier for seven other Patient groups.

Differentiated approvals result in a large number of patient groups

Dasabuvir is only approved in combination with other drugs (ombitasvir/paritaprevir/ritonavir and/or ribavirin). The Summaries of Product Characteristics specify partly different treatment regimens both for these drugs or drug combinations and for the respective comparator therapies. This results in as many as ten patient groups for this benefit assessment, which mainly differ in type of virus, pretreatment and stage of disease.

Two direct comparative studies

All ten groups were reflected in the dossier compiled by the drug manufacturer, but the data were informative for only three of these groups. The benefit assessment was based on two randomized controlled approval studies (MALACHITE I and II), in which dasabuvir in combination with ombitasvir/paritaprevir/ritonavir and/or ribavirin was directly compared with triple therapy consisting of telaprevir, pegylated interferon and ribavirin.

In compliance with the approval, the new fixed-dose combination was administered in the intervention arm for a period of 12 weeks, whereas treatment in the comparator arm could last up to 48 weeks, depending on response to the treatment.

Patients in the intervention arm were free of the virus more frequently

These two studies provided conclusive results for patients who have not yet developed cirrhosis of the liver and who are infected with a virus of genotype 1a or 1b. In genotype 1a, this applies both to treatment-naive patients and to patients who had relapsed after initially successful treatment. In genotype 1b, appropriate data were available only for treatment-naive patients.


In these three patient groups, the data showed a statistically significant difference in sustained virologic response (SVR) in favour of the new fixed-dose combination. IQWiG derived an indication of an added benefit from this. Its extent is non-quantifiable, however. It remained unclear in how many patients in whom the virus is no longer detectable, late complications, and liver cancer in particular, can actually be prevented.

Quality of life: advantage in treatment-naive patients

For the first time in the assessment of a hepatitis C drug, the manufacturer dossier contained evaluable data on health-related quality of life, which is of particular importance regarding interferon, which is considered to be very burdensome. These data on quality of life showed an advantage of dasabuvir at least for the duration of treatment. This applies to certain treatment-naive genotype 1a or 1b patients, but not to treatment-experienced patients (genotype 1a). It depends on the severity of the disease whether they have an advantage and how big this advantage is.

IQWiG derived a hint of an added benefit with differing extent from these data.

Data on side effects partly not conclusively interpretable

The important differences in treatment duration between intervention and control arm, which could be up to 36 weeks, partly made it impossible to interpret differences in side effects. Since the observation periods also differed, the results were probably biased.

Regarding the robustness of the data, however, there were exceptions in certain patient groups or aspects of side effects (serious adverse events and treatment discontinuation). In each case, the results were in favour of the new fixed-dose combination.

IQWiG therefore sees a hint or an indication of lesser harm in treatment-naive genotype 1b patients and an indication of lesser harm in treatment-experienced genotype 1a patients for individual aspects of side effects. Overall, greater or lesser harm is not proven.

Robust data were lacking for further patient groups

The dossier contained no suitable data for the remaining seven patient groups (genotype 1). Since direct comparative studies were lacking, the manufacturer referred to results on dasabuvir, in which the drug was not tested against the appropriate comparator therapy, however. No systematic comparison with data on the appropriate comparator therapy was conducted. Since there was also no systematic search for studies on the comparator therapies, it can be assumed that the data were incomplete.

Overall, an indication of a non-quantifiable added benefit can be derived from the dossier for three patient groups: patients without cirrhosis of the liver infected with genotype 1a (treatment-naive and treatment-experienced) and with genotype 1b who have not been pretreated.

G-BA decides on the extent of added benefit

This dossier assessment is part of the early benefit assessment according to the Act on the Reform of the Market for Medicinal Products (AMNOG) supervised by the G-BA. After publication of the dossier assessment, the G-BA conducts a commenting procedure and makes a final decision on the extent of the added benefit.

An overview of the results of IQWiG's benefit assessment is given by a German-language executive summary. In addition, the website » http://www.gesundheitsinformation.de, published by IQWiG, provides easily understandable German-language information.
More English-language information will be available soon (Sections 2.1 to 2.7 of the dossier assessment as well as subsequently published health information on » http://www.informedhealthonline.org). If you would like to be informed when these documents are available, please send an e-mail to » info@iqwig.de

HealthWell Foundation's New Fund Brings Financial Relief to Underinsured People Living with Hepatitis C

HealthWell Foundation's New Fund Brings Financial Relief to Underinsured People Living with Hepatitis C

Information contained on this page is provided by an independent third-party content provider. WorldNow and this Station make no warranties or representations in connection therewith. If you have any questions or comments about this page please contact pressreleases@worldnow.com.

SOURCE HealthWell Foundation

New Hepatitis C Fund - A Welcome Announcement During Hepatitis Awareness Month

GAITHERSBURG, Md., May 20, 2015 /PRNewswire/ -- The HealthWell Foundation®, an independent non-profit that provides a financial lifeline for inadequately insured Americans, today announced the launch of a new fund to assist people living with hepatitis C (also known as HCV).

Through the fund, the HealthWell Foundation will provide copayment assistance for HCV treatment, up to $15,000, to eligible patients who are insured and have annual household incomes up to 500 percent of the federal poverty level. According to the Centers for Disease Control and Prevention, one in 30 baby boomers has HCV.

"The new generation of hepatitis C treatments has brought excitement to patients who have been hoping for a breakthrough," said Krista Zodet, HealthWell Foundation President. "Through the generosity of our donors, our Hepatitis C Fund is able to help more people receive these treatments while minimizing the worry over financial stress."

"Nearly 3.2 million people in the United States and about 150 million people worldwide are chronically infected with HCV," said Tom Nealon, Esq., National Board Chair of the American Liver Foundation, a national patient advocacy organization that promotes education, support and research for the prevention, treatment and cure of liver disease. "The HealthWell Foundation and other independent copay charities play a vital role in seeing that those who are insured but can't afford their medication copay are able to access and stay on treatment."

According to BOOM!Health, a community service organization located in the Bronx, New York, 75 percent of those with HCV don't know it. The U.S. Preventive Services Task Force recommends screening for hepatitis C virus in persons at high risk for infection and a one-time screening for ALL adults born between 1945 and 1965 (baby boomers).

The most important risk factor for HCV infection is past or current injection drug use, with most studies reporting a prevalence of 50 percent or more. Many HCV infections are identified only after the patient becomes symptomatic. This makes the role of community health centers extremely important for getting patients into care.

"People living with HCV continue to face serious challenges, such as stigma and lack of access to treatment," said Robert Cordero, President and Chief Program Officer, BOOM!Health. "Non-profits that provide funding assistance like HealthWell fill a gap that we've watched grow."

To determine eligibility and apply for assistance through the HealthWell Foundation's Hepatitis C Fund, or to learn how you can support this program, visit the Foundation's website atwww.HealthWellFoundation.org.

About Hepatitis C

Hepatitis C is a disease that results from the hepatitis C virus (HCV) infecting the liver. The other common hepatitis viruses are A and B, which differ somewhat from HCV in the way they are spread and treated.

According to the American Liver Foundation, HCV usually produces no symptoms or very mild symptoms in the early stages. Many do not know they are infected until there is liver damage, which sometimes is discovered decades after being infected. HCV can be short-term, lasting up to six months (acute hepatitis C) or long-term (chronic) hepatitis C, which doesn't go away. About 75 to 85 percent of those infected by the hepatitis C virus will develop chronic HCV.

Other risk factors for contracting HCV in addition to sharing needles include:
Using unsterile equipment for tattoos or body piercings;
Coming in contact with infected blood or needles;
Receiving a blood transfusion or organ transplant before July 1992;
Receiving a blood product for clotting problems made before 1987;
Needing blood filtered by a machine (hemodialysis) for a long period of time due to kidney failure;
Being born to a mother with HCV;
Having unprotected sex with multiple partners;
Having or had a sexually transmitted disease; and,
Having HIV

About the HealthWell Foundation

A nationally recognized independent non-profit organization founded in 2003, the HealthWell Foundation® has served as a safety net for underinsured patients by providing access to life-changing medical treatments they otherwise would not be able to afford.

HealthWell provides financial assistance to adults and children facing medical hardship resulting from gaps in their insurance that cause out-of-pocket medical expenses to escalate rapidly. HealthWell assists these patients with their treatment-related cost-sharing obligations. To date, HealthWell has provided grant assistance to over 200,000 Americans totaling nearly $900 million.

For more information, please visit www.HealthWellFoundation.org.

CONTACT:
Ginny Dunn
240-632-5309
Ginny.Dunn@HealthWellFoundation.org

To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/healthwell-foundations-new-fund-brings-financial-relief-to-underinsured-people-living-with-hepatitis-c-300086245.html

MedPage Today HCV HOT TOPICS - 10 Day Video Series

MedPage Today HCV HOT TOPICS -  10 Day Video Series

MedPage Today invited specialists from leading medical institutions to weigh in on the latest advancements in hepatitis C with one question each day for 10 days.

(Post Dates Subject to Change)

Achillion partners with J&J to develop hepatitis C drugs

CORRECTED-UPDATE 

Achillion partners with J&J to develop hepatitis C drugsAchillion Pharmaceuticals Inc said it will collaborate with Johnson & Johnson to develop and market its hepatitis C drugs including an oral regimen that could work on all genotypes and shorten treatment time.

Achillion will be eligible for milestone payments of up to $1.1 billion related to the development, regulatory approval and sales of the drugs.

Johnson & Johnson will also invest $225 million in Achillion in return for about 18.4 million unregistered shares at $12.25 per share.

Achillion is developing three hepatitis C drugs -- ACH-3102 and sovaprevir in mid-stage trials and ACH-3422 in early-stage trials.

ACH-3102, which was granted fast-track designation in the United States, will be part of the oral regimen that could shorten treatment time to six weeks by 2018, the companies said on a call with analysts.

Gilead Sciences Inc's recently approved pill Harvoni requires at least eight weeks of treatment. The pill combines two of Gilead's other drugs - ledipasvir and sovaldi.

The fight against hepatitis C has made huge gains in recent years. A couple of years ago, patients needed 48 weeks of treatment with drugs that had harsh side effects. They cured only about 40 percent of patients.

The new all-oral treatments seek to replace injectable interferon and its flu-like side effects as well as an older drug called ribavirin that caused anemia and other problems.

Achillion's shares closed at $10.68 on the Nasdaq on Tuesday.

(Reporting by Amrutha Penumudi in Bengaluru; Editing by Don Sebastian)

High Cost of Hepatitis C Drug Prompts a Call to Void Its Patents

High Cost of Hepatitis C Drug Prompts a Call to Void Its Patents
By ANDREW POLLACK
MAY 19, 2015
Activists in several countries are seeking to void patents on the blockbuster hepatitis C drug Sovaldi, saying that the price being sought by the manufacturer, Gilead Sciences, was prohibitive. 
The Initiative for Medicines, Access and Knowledge, a legal group in New York, is expected to announce Wednesday that it has filed challenges in Argentina, Brazil, China, Russia and Ukraine. In all those countries except China, the organization is being joined by local patient advocacy groups.
Continue reading....



Tuesday, May 19, 2015

Audio - HCV Experienced Patients: Resistance testing, Cirrhosis and Genotype 3 Infection

New in May at Clinical Care Options (CCO)

On Monday "Clinical Care Options" released this comprehensive webinar; Practice-Changing Advances From EASL 2015, with Dr. Mark Sulkowski discussing the following topics; HCV therapy in the setting of renal impairment, resistance testing in DAA experienced patients, and the best approach to treat patients with cirrhosis or experienced patients who have genotype 3 infection.

Click below to listen, or download this 30 minute program with slides at Clinical Care Options.


EASL Highlights
Downloadable slides: Investigational agents and approved HCV therapies 

This downloadable slideset summarizes key studies selected by Andrew J. Muir, MD, David R. Nelson, MD, and Norah Terrault, MD, MPH, regarding the use of investigational agents for treating hepatitis C presented at the 2015 Annual Meeting of the European Association for the Study of the Liver.
Date Posted: 5/12/2015

Highlights From EASL: HCV Approved Therapies
In this downloadable slideset, Jordan J. Feld, MD, MPH; Kris V. Kowdley, MD, FACP, FACG, FASGE, AGAF, FAASLD; and Stefan Zeuzem, MD, review key studies on currently approved HCV therapies presented at the 2015 Annual Meeting of the European Association for the Study of the Liver.
Date Posted: 5/11/2015

Free registration is required