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LaunchPad Medical leitet erste europäische klinische Studie ein
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News provided by

LaunchPad Medical, Inc.

Jul 07, 2020, 17:52 ET

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LaunchPad Medical erhält die Genehmigung zum Beginn einer klinischen Studie seines Biomaterial-Knochenklebers im Bereich zahnmedizinischer Implantate in Großbritannien

LOWELL, Massachusetts, 7. Juli 2020 /PRNewswire/ -- LaunchPad Medical Inc. hat bekannt gegeben, dass man von der britischen Gesundheitsbehörde „Medicines and Healthcare products Regulatory Agency" die Genehmigung zum Start einer klinischen Pilotstudie mit 15 Patienten zur Untersuchung der Sicherheit und Wirksamkeit von Tetranite® erhalten hat, dem Biomaterial-Knochenkleber des Unternehmens zur sofortigen Stabilisierung von Zahnimplantaten nach einer Zahnextraktion.

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This study will focus specifically on the use of the company’s bone adhesive biomaterial to immediately stabilize dental implants following the extraction anterior teeth located in the aesthetic or “smile” region where the loss of a tooth is highly visible. Unlike the company’s ongoing clinical study in the United States, patients in this study will also receive temporary crowns at the time their implants are placed.
This study will focus specifically on the use of the company’s bone adhesive biomaterial to immediately stabilize dental implants following the extraction anterior teeth located in the aesthetic or “smile” region where the loss of a tooth is highly visible. Unlike the company’s ongoing clinical study in the United States, patients in this study will also receive temporary crowns at the time their implants are placed.

Diese Studie wird sich speziell auf Vorderzähne konzentrieren, die sich im ästhetisch wichtigen Bereich befinden, in dem eine Zahnlücke extrem sichtbar ist. Anders als in der laufenden klinischen Studie des Unternehmens in den Vereinigten Staaten werden Patienten in dieser Studie zum Zeitpunkt der Platzierung der Implantate vorübergehend Kronen erhalten. Die Verwendung von Tetranite wird bei vielen Patienten eine teure, komplexe und langwierige Knochenverpflanzung überflüssig machen und den Zeitraum der Behandlung stark verkürzen.

Dr. Michael R. Norton, BDS, FDS, RCS(Ed), ein Kieferchirurg aus London, bekannter Dozent und früherer Präsident der internationalen Academy of Osseointegration, wird Hauptprüfarzt der Studie. „Ich bin höchst erfreut, der erste Arzt außerhalb der Vereinigten Staaten zu sein, der diese bahnbrechende Technologie zur Verbesserung der Versorgung der Patienten und Beschleunigung der Restaurierung ihres Gebisses verwendet", sagte Dr. Norton. „Ich bin der Überzeugung, dass diese Technologie die Art und Weise der Platzierung dentaler Implantate revolutionieren wird."

„Wir sind sehr angetan davon, unsere erste Studie außerhalb der Vereinigten Staaten einleiten zu können", sagte Brian Hess, der CEO von LaunchPad Medical. „Zudem erfüllt die Zusammenarbeit mit Dr. Norton, einem Vordenker der Weiterentwicklung klinischer Praxis im Feld der zahnmedizinischen Implantate, uns mit Zuversicht."

Informationen zu LaunchPad Medical Inc.

LaunchPad Medical Inc. ist ein Medizinproduktehersteller, der einen patentierten, synthetischen, injizierbaren, selbstaushärtenden und osteokonduktiven Biomaterial-Knochenkleber namens Tetranite® entwickelt und vermarktet. Anfänglich liegt der Schwerpunkt für diese Technologie beim Einsatz in der Dentalbranche. Das Unternehmen befasst sich zudem mit der Entwicklung von Klebungsawendungen im breiteren Orthopädiemarkt. Die Tetranite-Technologie von LaunchPad Medical wurde noch nicht zur kommerziellen Verwendung zugelassen.

Foto - https://mma.prnewswire.com/media/1201446/LaunchPad_Medical_European_Clinical_Study.jpg  

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