Project Details
Description
Bayer 20414: A multicenter, non-randomized, open-label, multiple dose escalation study to evaluate the safety and tolerability of subcutaneous BAY 1093884 in males with hemophilia
Status | Finished |
---|---|
Effective start/end date | 3/11/19 → 3/30/24 |
Funding
- BAYER HEALTHCARE PHARMACEUTICALS
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