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Surveyed Hematologists in China Expect the Market Entry of Generic Imatinib to Significantly Decrease Glivec’s Patient Share in Chronic Myeloid Leukemia

June 2, 2014

High Cost and High Expectations for Clinical Benefits are Major Market Access Hurdles Facing New CML Therapies, According to Findings from Decision Resources Group

BURLINGTON, Mass., June 2, 2014 /PRNewswire/ — Decision Resources Group finds that surveyed hematologists in China estimate that Novartis’s Glivec (imatinib) will lose nearly half of its patient share for treatment of chronic myeloid leukemia (CML) in the next three years, due to the market entry of generic imatinib. Nevertheless, imatinib (Glivec and generics) will continue to dominate the market for first-line chronic phase CML. There will be continued uptake of Novartis’s Tasigna and Bristol-Myers Squibb’s Sprycel, and new therapies such as Pfizer’s Bosulif and Jiangsu Hansoh’s flumatinib will gain a foothold for second- and third-line accelerated or blast phase CML. However, the expected high cost of new agents and lack of reimbursement are significant hurdles for drug uptake.

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Other key findings from the Emerging Markets Physician & Payer Forum report entitled Patient Access to High Cost Therapies for CML in China: How are Payers and Physicians Shaping this Crowded and Changing Market:

    --  Additional market access hurdles: The increasingly crowded market and
        high expectations for clinical benefits, as well as surveyed physicians'
        low familiarity with emerging CML agents, are also major access
        obstacles for emerging therapies. Levers to circumvent these hurdles are
        discussed in the report.
    --  Drug choices for BCR-ABL mutations: Hematologists indicated that half of
        the patients undergoing BCR-ABL mutation analysis have a mutation, with
        the most common one being T315I. Tasigna and Sprycel are preferred for
        various mutation sites respectively; however, none of them are sensitive
        to T315I.
    --  Market entry of generics: If generics are proven to be equivalent to the
        branded drugs in terms of both efficacy and safety, they will make
        significant gains in market share over the next three years, according
        to surveyed hematologists. The addition of generics may also drive down
        the cost of branded drugs, thus increasing the chances for inclusion in
        provincial/national formularies.

Comments from Decision Resources Group Analyst Michelle Zhou, M.B.B.S., Ph.D.:

    --  "High-cost tyrosine kinase inhibitors (TKIs) have dominated the China
        CML market. According to surveyed hematologists, more than 60 percent of
        their patients at any stage of disease receive TKIs. However, their high
        cost and the lack of reimbursement remain important hurdles for uptake.
        Market entry of generics is anticipated to become a threat to the
        current branded TKIs but will increase the penetration of this class
        within the CML market space."
    --  "Existing CML drugs have shown good efficacy and safety, except for some
        unique mutation sites such as T315I--this represents a clear unmet need
        in CML treatment. In order to maximize market share in this crowded
        market, it is vital for new drugs to show superior benefits or target
        new mutation sites, especially when generics begin to join this
        competition and further differentiation of the branded agents will be
        required."

About Decision Resources Group

Decision Resources Group offers best-in-class, high-value information and insights on critical issues within the healthcare industry. Clients rely on this analysis and data to make informed decisions. Find out more at www.DecisionResourcesGroup.com.

All company, brand, or product names contained in this document may be trademarks or registered trademarks of their respective holders.

For more information, contact:

Decision Resources Group

Christopher Comfort

781-993-2597

ccomfort@dresourcesgroup.com

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SOURCE Decision Resources


Source: PR Newswire



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