Clinuvel reports positive results in Phase III EPP trial
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Earlier from Clinuvel Pharmaceuticals
- FDA provides positive guidance on Clinuvel`s EPP program
- EMA acknowledges Clinuvel filing afamelanotide in Europe `11
- Clinuvel records first A$1 million in sales
- Clinuvel presents SCENESSE to global porphyria conference
- Clinuvel granted Australian formulation patent
Later from Clinuvel Pharmaceuticals
- SCENESSE attains breakthrough European Market Authorisation
- SCENESSE Treatment in Europe
- SCENESSE launched in Europe
- FDA awards SCENESSE Fast Track designation for EPP treatment
- FDA accept SCENESSE clinical data package for NDA submission
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