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GlaxoSmithKline Presents Innovative Neuroscience Pipeline
Date:12/13/2007

from this study are anticipated in 2009.

Other pipeline news:

At the seminar today, GSK also provided an update on progress made this year on its overall pipeline. So far in 2007, the company has gained 8 key approvals, submitted 8 regulatory filings and started new phase III trials for 9 key assets:

Key Approvals Filings Phase III commenced

Altabax/Altargo Avodart plus alpha 1838262 (RLS)

(US & EU) blocker co-prescription

(US & EU)

Arixtra ACS (EU) Cervarix (US) Belimumab (SLE)

Veramyst (US) Gepirone ER (US) Elesclomol (STA-

4783) (melanoma)

Cervarix (EU) H5N1 (EU) MAGE-A3 therapeutic

vaccine (NSCLC)

ReQuip XL (EU) Lunivia (EU) MenACWY-TT meningitis

vaccine

Seretide TORCH Volibris (EU) Ofatumumab (RA)

(EU)

Tykerb (US) Requip XL (PD) (US) Promacta (hep c)

Wellbutrin XR (EU) Rotarix (US) Tykerb (H&N cancer)

Tykerb + Pazopanib

(IBC)

Before year-end, GSK will submit a regulatory filing to the FDA for Promacta, its first-in-class, oral platelet growth factor, for short-term treatment of patients with idiopathic thrombocytopaenic purpura, a condition which results in low blood platelet counts and bleeding from the small blood vessels. The company also confirmed that it expects to file the vaccine Synflorix with European and International regulatory authorities by the end of the year. The vaccine is designed to protect against pneumococcal disease and otitis media caused by non-typeable Haemophilus influenzae (NTHi). Otitis media is a major burden
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SOURCE GlaxoSmithKline
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