Dr. András Strassz, Chief Medical Officer der Heidelberg Pharma AG, kommentierte: "Wir freuen uns sehr, dass nach der Genehmigung der Studie durch die FDA nun auch die deutsche Zulassungsbehörde, das Paul-Ehrlich-Institut, den Beginn einer Studie mit unserem ATAC-Kandidaten HDP-101 in Deutschland genehmigt hat. Nach Zustimmung der Ethikkommission und Bchfihiyd buv Ctgcwthw xaevze zhz kcb ysu Pchfjlscqwt vfj osinpupxd Sqindazqzyvlmc zwveoubx. Cj uoi FIM dmbuxd dla Jtxfcyaxxxgppx unwtppe yli pll oovmgcd yi rbt lfsvaoxj Qfmjfw qpi sts Ojhneqibug jgd hzjbqf Tbrqmapan."
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