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NeoSpect (depreotide)

Region
🇪🇺 EU
Active substance
depreotide
Company
CIS bio international
Status
Withdrawn
Therapeutic area
Radionuclide Imaging
EU approval
Wed 29 Nov 2000
Application
EMEA/H/C/000263
ATC
V09IA05
Official record
www.ema.europa.eu

Indication

This medicinal product is for diagnostic use only.For scintigraphic imaging of suspected malignant tumours in the lung after initial detection, incombination with CT scan or chest X-ray, in patients with solitary pulmonary nodules.

Regulatory milestones

No milestones recorded in the last year.

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.