Vicore Pharma Holding AB

Vicore Pharma Holding AB
About Us
Change country

Follow us:
Share:
Subscribe:

About Us

Vicore is a rare disease pharmaceutical company focused on rare lung disorders and related indications. The company currently has three drug development programs, VP01, VP02 and VP03.VP01 aims to develop the substance C21 for the treatment of idiopathic pulmonary fibrosis (“IPF”), pulmonary fibrosis in systemic sclerosis (“SSc”) and COVID-19. VP02 is based on a new formulation and delivery route of an existing immunomodulatory compound (an “IMiD”). VP02 focuses on the underlying disease and the severe cough associated with IPF. VP01 and VP02 are also being actively evaluated for other indications within the field of interstitial lung diseases which have a significant unmet need. VP03 includes follow-up molecules to VP01. The company's shares (VICO) are listed on Nasdaq Stockholm’s main market. For more information, see www.vicorepharma.com.

Pick a time period -

Tags ( Active)

All Regulatory Non-Regulatory

Update on progress in clinical lead program VP01 (C21)

Tue, Oct 01, 2019 08:00 CET

Gothenburg, October 1, 2019 – Following the successful dose escalation phase I study, Vicore Pharma Holding AB (publ), a pharmaceutical company dedicated to developing innovative medicines for rare lung disorders, today announces an update with regards to its clinical lead program VP01 (C21) and confirms progress according to plan.A phase II CTA (clinical trial application) has been filed with the MHRA, the regulatory body in the UK, for studying the effect of a single dose of C21 on cold induced vasoconstriction in subjects with systemic sclerosis (SSc). “This study will enable us to

Results from extension study with C21 show safety, tolerability and indicate effects on lipid metabolism

Thu, Aug 17, 2017 08:50 CET

Vicore Pharma AB (publ) (ticker: VICO) can today announce positive results from the Phase I extension study with its candidate drug C21.The extension study, initiated in January 2017, was performed on a group of overweight men (BMI 30-35) and with a hip to waist ratio below 0.9 but otherwise healthy. In total 16 volunteers, whereof 8 were given 100 mg C21 and 8 were given placebo during a period of 8 days participated. The aim of the study was to evaluate safety and tolerability of C21 in a group with a potentially compromised metabolic situation and to investigate if markers of metabolic

Vicore Pharma is granted orphan drug designation from FDA for the treatment of IPF

Fri, Jan 27, 2017 11:46 CET

US Food and Drug Administration (FDA) has granted orphan drug status for Vicore Pharma's lead compound C21 for the treatment of idiopathic pulmonary fibrosis (IPF). FDA has granted orphan drug designation for Vicore Pharma's drug candidates C21 for the treatment of IPF. C21 is thereby approved as an orphan drug in the USA. The approval brings C21 exclusivity on the US market from when the drug will be approved and for 7 years thereafter. Other benefits related to orphan drug designation include tax relief on the costs for clinical trials executed in the USA and support from the

There are no items matching the current filter

There are no more items matching the current filter

Share

About Us

Update on progress in clinical lead program VP01 (C21)

Results from extension study with C21 show safety, tolerability and indicate effects on lipid metabolism

Vicore Pharma is granted orphan drug designation from FDA for the treatment of IPF

Media