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Company profile

Intrabio Inc

UK company FC034088, incorporated on 1 January 2017.

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IntraBio is a leader in discovering, developing, and commercializing novel therapies and treatments for rare and neurodegenerative diseases with high unmet medical needs.

Company number
FC034088
Incorporated
1 Jan 2017
Companies House status
Active

Company identity

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Founded / incorporated
1 January 2017

Company number FC034088

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Legal name
INTRABIO INC
Company type
OVERSEA-COMPANY
Region
Unknown
Registered address
Unknown
Insolvency history
No

Company events

Reference milestones and recent Companies House filing stream events.

1 event
01 Jan
2017

Incorporated

Inception

Company registered at Companies House

Spinout profile

2 entries

Company description

Intrabio specializes in developing and discovering novel therapies and treatments aimed at helping those with rare and neurodegenerative diseases with high unmet medical needs.

Project impact

Successful Phase III trial In this double-blind, placebo-controlled, crossover trial, we randomly assigned patients 4 years of age or older with genetically confirmed Niemann-Pick disease type C in a 1:1 ratio to receive N-acetyl-L-leucine (NALL) for 12 weeks, followed by placebo for 12 weeks, or to receive placebo for 12 weeks, followed by NALL for 12 weeks. NALL met its primary SARA endpoint (least-squares mean difference, -1.28 points; 95% confidence interval, -1.91 to -0.65; P<0.001) and its secondary endpoints. NALL was well-tolerated, with no serious adverse reactions. N Engl J Med 2024; 390:421-431

Successful Phase III trial In this double-blind, placebo-controlled, crossover trial, we randomly assigned patients 4 years of age or older with genetically confirmed Niemann-Pick disease type C in a 1:1 ratio to receive N-acetyl-L-leucine (NALL) for 12 weeks, followed by placebo for 12 weeks, or to receive placebo for 12 weeks, followed by NALL for 12 weeks. NALL met its primary SARA endpoint (least-squares mean difference, -1.28 points; 95% confidence interval, -1.91 to -0.65; P<0.001) and its secondary endpoints. NALL was well-tolerated, with no serious adverse reactions. N Engl J Med 2024; 390:421-431 FDA approved lead compound Aqneursa for NPC on 27 September 2024

Intrabio Inc
2024
Intrabio Inc
2024