A STUDY TO ASSESS THE LONG-TERM SAFETY AND EFFICACY OF INTRAVENOUS ATB200 CO-ADMINISTERED WITH ORAL AT2221 IN ADULT SUBJECTS WITH LATE-ONSET POMPE DISEASE

A  STUDY TO ASSESS THE LONG-TERM SAFETY AND EFFICACY OF INTRAVENOUS ATB200 CO-ADMINISTERED WITH ORAL AT2221 IN ADULT SUBJECTS WITH LATE-ONSET POMPE DISEASE
Enrolling By Invitation
18 years - 99 years
All
Phase 3
3 participants needed
1 Location

Brief description of study

A STUDY TO ASSESS THE LONG-TERM SAFETY AND EFFICACY OF INTRAVENOUS ATB200 CO-ADMINISTERED WITH ORAL AT2221 IN ADULT SUBJECTS WITH LATE-ONSET POMPE DISEASE

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: POMPE DISEASE,POMPE DISEASE
  • Age: 18 years - 99 years
  • Gender: All

completion of study ATB200-03 Male Female over age 18

Updated on 04 Aug 2024. Study ID: 843492
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Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

Contact Office of Clinical Research