Drug Profile


Alternative Names: TXA 127

Latest Information Update: 20 Jan 2017

Price : $50

At a glance

  • Originator Tarix Orphan; Tarix Pharmaceuticals
  • Developer Tarix Orphan; Tarix Pharmaceuticals; Unigene Laboratories; US Biotest Inc
  • Class Antihypertensives; Heart failure therapies; Peptide hormones
  • Mechanism of Action Haematopoietic cell growth factor stimulants; Proto-oncogene protein c-mas-1 agonists; Transforming growth factor beta modulators
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Epidermolysis bullosa; Pulmonary arterial hypertension; Limb girdle muscular dystrophies; Muscular dystrophies; Duchenne muscular dystrophy; Stem cell engraftment; Myelodysplastic syndromes
  • On Fast track

    Fast track status is assigned by the US FDA so therapies with the potential to address unmet needs can move faster through development.

    Duchenne muscular dystrophy; Muscular dystrophies
  • New Molecular Entity No

Highest Development Phases

  • Preclinical Amyotrophic lateral sclerosis; Connective tissue disorders; Duchenne muscular dystrophy; Epidermolysis bullosa; Limb girdle muscular dystrophies; Muscular dystrophies
  • Discontinued Adult respiratory distress syndrome; HIV infections; Peripheral vascular disorders; Pulmonary arterial hypertension; Stem cell engraftment; Stroke; Thrombocytopenia

Most Recent Events

  • 18 Jan 2017 Angiotensin-1-7 receives rare paediatric disease designation status for Epidermolysis bullosa in USA
  • 07 Sep 2016 Angiotensin-1-7 receives Orphan Drug status for Epidermolysis bullosa in USA
  • 27 Jun 2016 Preclinical trials in Epidermolysis bullosa in Germany (SC)
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