3 results
The primary objective of this study is to evaluate the efficacy of TDF plus Peginterferon *-2a (PEG) combination therapy for 48 weeks versus standard of care TDF monotherapy or PEG monotherapy for 48 weeks in non-cirrhotic CHB subjects as determined…
PRIMARY* To determine the efficacy on study Day 28 of T-Guard in inducing a clinical response in patients with severe acute GVHD refractory to first line steroid therapy.SECONDARY* To evaluate the overall safety and efficacy during the first 6…
1. Are telemedicine and FTF-evaluation similar?2. Are TM-evaluation from a general practitioners office and FTF-evaluation similar? 3. How do parents/patients value the TM evaluation?4. How do general practitioners and paediatricians value the TM…