WHO ICTRP trial

A single center, open-label, dose escalation study of the safety and…

EUCTR2010-022084-36-DK · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2010-022084-36-DK
Public title A single center, open-label, dose escalation study of the safety and pharmacokinetics of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) for the treatment of patients with alpha-mannosidosis.
Scientific title A single center, open-label, dose escalation study of the safety and pharmacokinetics of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) for the treatment of patients with alpha-mannosidosis.
Primary sponsor Zymenex A/S
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Countries Denmark
Conditions Treatment of alpha-Mannosidosis
Interventions Product Name: Lamazym Product Code: rhLAMAN Pharmaceutical Form: Solution for infusion INN or Proposed INN: recombinant human alpha-mannosidase Current Sponsor code: rhLAMAN Concentration unit: mg/ml milligram(s)/millilitre Concentration…
Registration date Aug 20, 2010
Target size 10
Secondary IDs rhLAMAN-02
Registry page clinicaltrialsregister.eu

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