リボミック、軟骨無形成症の治療薬RBM-007の治験計画書を提出 / RIBOMIC, Completion of IND submission of RBM-007 for Treatment of Achondroplasia

リボミック、軟骨無形成症の治療薬RBM-007の治験計画書を提出 / RIBOMIC, Completion of IND submission of RBM-007 for Treatment of Achondroplasia

リボミック(本社、東京都港区)は、軟骨無形成症の誘導因子と考えられるFGF2の機能を特異的かつ強力に阻害する治療薬(RBM-007)を用いた新薬の治験計画届書を(独)医薬品医療機器総合機構(PMDA)に提出したことを2020年4月9日(JST)に発表しました。

今後、30日間の間、PMDAより保留に関わる通達がない場合、同社は第Ⅰ相臨床試験を実施することができます。実施施設は日本国内で1施設、被験者となる健康な成人男性は24人となる見込みです。詳細は同社のリリースをご参考ください。

RIBOMIC, Inc. (HQ, Minato-ku, Tokyo) announced on April 9th, 2020 (JST) that it submitted an Investigational New Drug Application (IND) to the Pharmaceuticals and Medical Devices Agency (PMDA) in Japan to test its novel drug RBM-007 which has been shown to have potent effects in limiting excessive interactions between fibroblast growth factors, which are known to cause Achondroplasia.

RIBOMIC expects to begin phase 1 clinical trial, without any notices from PMDA, at a single site in Japan with a total of 24 healthy adult males. Please refer to the source for their details.

Source: RIBOMIC website

Japanese https://ssl4.eir-parts.net/doc/4591/tdnet/1814889/00.pdf

English https://ssl4.eir-parts.net/doc/4591/announcement6/57673/00.pdf

コメントを残す

Follow

Get every new post on this blog delivered to your Inbox.

Join other followers: