burosumab-twza (crysvita) Report issue

Biologics mAb Orphan Drug FDA Approved FDA Fast Track FDA
AACT ChEMBL Drugs@FDA

Active Ingredient History

NOW
  • Now
Burosumab, sold under the brand name Crysvita, is a human monoclonal antibody medication approved 2018 for the treatment of X-linked hypophosphatemia and tumor-induced osteomalacia.   Wikipedia

Chemistry

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Pharmacology

  • Mechanisms of Action:
  • Multi-specific: No
  • Black Box: No
  • Availability: Missing data
  • Delivery Methods: Missing data
  • Pro Drug: No

Drug Pricing (per unit)

United States

$2556.3900 - $10183.8700
More Pricing Detail

Note: This drug pricing data is preliminary, incomplete, and may contain errors.

Alternative names

burosumab | burosumab-twza | krn23 | krn-23

Organizations (11)

Research & Development (11)

Organization Org Type FDA approvals Clinical Trials involvement Org ID Force Sort

Marketing (2)

Organization Org Type FDA approvals Clinical Trials involvement Org ID Force Sort

Indications (8)

Approved Indications (0)

Experimental Indications - Clinical Trial Phases 1-4 (8)


 

Chronic Pain (Phase 3)

Familial Hypophosphatemic Rickets (Phase 4)

Genetic Diseases, X-Linked (Phase 3)

Hypophosphatemia (Phase 3)

Neoplasms (Phase 2)

Nevus (Phase 4)

Rare Diseases (Phase 4)

Rickets, Hypophosphatemic (Phase 3)

Overview

  • Highest Phase: Phase 4
  • # of Trials: 28
  • # of Trial Organizations: 11

Trials by Phase

Trial Phase Start Date Organizations Indications

Feedback

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