EICHORCondition: Pompe Disease · Sponsor: Shionogi
The primary purpose of this study is to evaluate the long-term safety and tolerability profile of S-606001 in participants with LOPD. Participants who completed other S-606001 studies (for example, NCT07123155), including participants in a S-606001 study whose allocated arm was terminated by the sponsor and who are willing to participate in this study, will be enrolled globally.
This description comes directly from the study's public registry record.
Shionogi Clinical Trials Administrator Clinical Support Help Line · 1-800-849-9707 · Shionogiclintrials-admin@shionogi.co.jp
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| Locations not yet listed on the registry record. |
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Source record: clinicaltrials.gov/study/NCT07750990