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Indimacis 125 (igovomab)

Region
🇪🇺 EU
Active substance
igovomab
Company
CIS bio international
Status
Withdrawn
Therapeutic area
Radionuclide Imaging; Ovarian Neoplasms
EU approval
Fri 04 Oct 1996
Application
EMEA/H/C/000065
ATC
V09IB03
Official record
www.ema.europa.eu

Indication

Positive diagnosis of relapsing ovarian adenocarcinoma when serum CA 125 is increased without positive results of ultrasound or computerised tomography scan.

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.