Alle Storys
Folgen
Keine Story von Zeltia Group mehr verpassen.

Zeltia Group

Zeltia Announces Third Quarter 2004 Financial Results

Madrid (ots/PRNewswire)

The Zeltia Group (ZEL.MC) today reported
financial results for the third quarter and the nine months ended
September 30, 2004.
Q3 Highlights
Financial:
  • Group sales up 6.3% to Euro 63.7million (Euro 59.9 million 9M03)
  • Losses before interest and tax narrowed significantly to Euro 2.3 million (Euro 5.5 million 9M03)
  • R&D down by 28.9% to Euro 27.8 million reflecting a reduction in early phase R&D expenditure at PharmaMar
  • Net cash of Euro 85 million as at September 30, 2004 (Cash + Cash equivalents - short term bank loans)
Operational:
  • FDA awarded orphan drug designation to Yondelis for the treatment of soft-tissue sarcoma
  • FDA awarded orphan drug designation to Aplidin for the treatment of multiple myeloma
  • Private placement of 25% of NeuroPharma completed, raising Euro 16 million

Contact:

Isabel Lozano, CEO, PharmaMar, S.A., Tel. +34-91-846-60-00. Catherine
Moukheibir, Head of Capital Market Strategy, Zeltia, S.A Tel.
+34-91-444-45-00. Ma. Luisa de Francia, CFO, Zeltia, S.A. Tel.
+34-91-444-45-00

Weitere Storys: Zeltia Group
Weitere Storys: Zeltia Group
  • 07.10.2004 – 08:30

    The FDA has Granted Orphan Drug Status to Yondelis for the Treatment of STS

    Madrid (ots/PRNewswire) - The United States Food & Drug Administration (FDA) has granted Orphan Drug Designation to Yondelis in the indication of Soft Tissue Sarcoma (STS). The sponsor of this application in the US is our partner Johnson & Johnson Pharmaceutical Research & Development. The European Commission (E.C.) already granted Orphan Drug status for this ...

  • 06.10.2004 – 08:43

    FDA Grants Aplidin(R) Orphan Drug Status for the Treatment of Multiple Myeloma

    Madrid, Spain (ots/PRNewswire) - PharmaMar announced today that Aplidin(R), its second marine-derived compound in Phase II clinical development, has been granted orphan drug status by the United States (US) Food and Drug Administration (FDA), for the treatment of Multiple Myeloma (MM). This is the second orphan drug designation granted to Aplidin by the FDA. The ...