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XARACOLL Market Size, Forecast, and Market Insight - 2032
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"XARACOLL Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about XARACOLL for Postoperative pain in the seven major markets. A detailed picture of the XARACOLL for Postoperative pain in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2019 -2032 is provided in this report along with a detailed description of the XARACOLL for Postoperative pain. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the XARACOLL market forecast analysis for Postoperative pain in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Postoperative pain.

Drug Summary:

XARACOLL (bupivacaine HCl) is a unique, non-injectable drug-device combination in the form of a fully bioresorbable collagen implant containing bupivacaine hydrochloride. XARACOLL is placed directly into the surgical site during surgery; after placement, it releases bupivacaine immediately, over time. It is indicated in adults for placement into the surgical site to produce postsurgical analgesia for up to 24 h following open inguinal hernia repair. As per the company, XARACOLL will be launched through a partnership between Mallinckrodt Pharmaceutical's acute care sales team and Innocoll's hospital sales team.

In March 2022, Innocoll Pharmaceuticals Limited announced positive topline results from Study INN-CB-024, a Phase III randomized, double-blind, placebo-controlled study evaluating the safety and efficacy of a 300 mg dose of XARACOLL, an innovative collagen drug-device implant, in patients undergoing abdominoplasty. As per the company, these positive topline Phase III results will support further development program and its anticipated sNDA application to expand the indications for XARACOLL.

Dosage and administration

XARACOLL is intended for single-dose administration. The recommended dose of XARACOLL is 300 mg (3 x 100 mg implants).

Scope of the Report:

The report provides insights into:

Methodology:

The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.

XARACOLL Analytical Perspective by DelveInsight

This report provides a detailed market assessment of XARACOLL for Postoperative pain in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2024 to 2032.

The report provides the clinical trials information of XARACOLL for Postoperative pain covering trial interventions, trial conditions, trial status, start and completion dates.

Report Highlights:

Key Questions:

Table of Contents

1. Report Introduction

2. XARACOLL Overview in Postoperative pain

3. Competitive Landscape (Marketed Therapies)

4. Competitive Landscape (Late-stage Emerging Therapies)

5. XARACOLL Market Assessment

6. SWOT Analysis

7. Analysts' Views

8. Appendix

9. DelveInsight Capabilities

10. Disclaimer

11. About DelveInsight

12. Report Purchase Options

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