was in-licensed from Novartis in 1999 and
licensed-back to Novartis Pharma in 2002 for further development
and commercialisation; SPP100 was approved by the FDA in the US in
March 2007, and filed by Novartis with the EMEA in the EU in Q3
2006. Our pipeline covers three different modes of action, and in
addition to SPP100, includes SPP301 in Phase III (on hold), SPP200
in Phase II, SPP635 in Phase Il, SPP1148 in Phase I and several
pre-clinical projects.
Speedel develops novel product candidates through focused
innovation and smart drug development from lead identification to
the end of Phase II. We either partner with big pharma for Phase
III and commercialisation in primary-care indications, or we may
ourselves complete Phase III development in specialist indications.
Candidate compounds for development and the company's intellectual
property come from our late-stage research unit Speedel Experimenta
and from in-licensing. Our team of approximately 70 employees,
including over 30 experienced pharmaceutical scientists, is located
at our headquarters and laboratories in Basel, Switzerland and at
offices in New Jersey, USA and Tokyo, Japan.
In January 2007 the company raised gross proceeds of CHF 55.5
million (approximately EUR 34.3 million or USD 44.5 million)
through a convertible bond issue. In March 2006 the company raised
gross proceeds of CHF 83.95 million (approximately EUR 53m or USD
64m) through the public offering of 500,000 treasury shares.
Previously, as a private company, we raised gross proceeds of CHF
255 million (approximately EUR 157 million or USD 204 million) from
private placements of equity securities and two convertible loans
including the conversion premiums. We have had total revenues,
principally from milestone payments, of CHF 57.7 million
(approximately EUR 37 million or USD 44 million). The company's
shares were listed in September 2005 on the SWX Swiss Exchange
under the symbol SPPN.
Forward lookin
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