Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Anika’s Orthovisc

This article was originally published in The Gray Sheet

Executive Summary

J&J Ortho Biotech will launch the injectable hyaluronic acid product for knee osteoarthritis pain in the U.S. following PMA approval, announced Feb. 5. Maker Anika Therapeutics will receive a $20 mil. milestone payment this quarter under a December domestic marketing agreement. Anika estimates the U.S. viscosupplementation market at $350 mil. J&J plans a launch "over the next few months" after a roll-out at the March 10-14 American Academy of Orthopaedic Surgeons meeting in San Francisco. Orthovisc has been available internationally since 1996. An initial PMA was rejected by FDA in 1998, leading to two additional studies and a revised PMA (1"The Gray Sheet" June 9, 2003, p. 27). Competitors include Genzyme Biosurgery's Synvisc, Smith & Nephew's Supartz and Fidia Pharmaceuticals' Hyalgan...

You may also be interested in...



Orthovisc Clinical Trial Data Filed With FDA; Will Third Time Prove A Charm?

Anika Therapeutics will seek a marketing partner to distribute its Orthovisc injectable hyaluronic acid if the knee osteoarthritis therapy is approved by FDA

As Casgevy, Lyfgenia Launches Proceed, CRISPR And bluebird bio CEOs Reassure

The CEOs of bluebird bio and CRISPR Therapeutics hope to inspire investor confidence that their gene-based therapies for sickle cell disease and beta thalassemia will be widely reimbursed in the US and EU.

Japan Regulatory Update: Revised Law Widens RWD Scope, Price Revisions/Listings

Japan now allows pseudonymized personal data for medical use under a licensing system for wider use of real-world data. Meanwhile, a national cost-effectiveness assessment scheme has slashed reimbursement prices for Lagevrio and Kerendia, and Alexion’s Voydeya has been added to the reimbursement tariff.

Latest Headlines
See All
UsernamePublicRestriction

Register

MT019693

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel