The Institute for Clinical and Economic Review (ICER) yesterday released a Draft Evidence Report assessing the clinical effectiveness and value of two new technologies to induce immune tolerance — Viaskin Peanut, from French allergy specialist DBV Technologies (Euronext Paris: DBV)) and AR101 from US biotech firm Aimmune Therapeutics (Nasdaq: AIMT) — as well as non-commercialized oral immunotherapy (OIT).
This draft report, wich questions the cost effectiveness of the products, will be open to public comment until 5pm ET on May 8, 2019. Based on stakeholder feedback, the ICER may revise key assumptions and findings for its Evidence Report, which will be published on May 28, 2019.
The Evidence Report will be subject to deliberation during a public meeting of the California Technology Assessment Forum ( CTAF), one of ICER’s three independent evidence appraisal committees, on June 11, 2019.
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