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Abonner Zeltia Group

Zeltia Group

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  • 26.10.2006 – 15:46

    Third Quarter 2006 Results

    Madrid, Spain (ots/PRNewswire) - - Zeltia Revenues up 10% and R&D Expenditure Rises 19% - Net Revenues Amounted To 64.3 Million Euro - Research and Development Expenditure Amounted to 36.8 Million Euro Zeltia S.A. (ZEL SM; ZEL MC) reported 64.3 million euro in net revenues in the first nine months of 2006, a 10% increase on the same period of 2005 (58.3 million euro). Research and development expenditure increased by 19% year-on-year to 36.8 million ...

  • 27.07.2006 – 14:01

    Zeltia S.A.: Report at 30 June 2006

    Madrid, Spain (ots/PRNewswire) - Corporate: - Zeltia performs 1-for-50 bonus issue - Group revenues amounted to 42.5 million euro. - Investment in R&D amounted to 24.4 million euro in the first half of 2006. - The net cash position (cash + cash equivalents + current financial assets - short-term borrowings) amounted to 55.3 million euro. PharmaMar: - Excellent results of Yondelis in myxoid ...

  • 05.06.2006 – 08:50

    Three New Key Studies at ASCO Highlight Antitumoral Activity of Yondelis(R)

    Atlanta, Georgia (ots/PRNewswire) - - 86% Rate of Tumour Control in myxoid liposarcomas - Correlation Between DNA Repair Gene Expression and Response Rate in Sarcomas - 78% Rate of Tumour Control in Platinum Pretreated Ovarian Cancer Patients PharmaMar highlights the results of three important studies out of 10 presented on Yondelis(R) at the Annual ...

  • 27.04.2006 – 09:24

    Zeltia Increases R&D Investment by 32.2% in the First Quarter 2006

    Madrid (ots/PRNewswire) - - Revenue Amounted to 14.8 Million Euros - Marketing Expenditure Increased 52.1% to 5.1 Million Euros - The Group Invested 11.8 Million Euros in Research and Development, Up 32% Zeltia S.A. (ZEL SM; ZEL MC) today presented its financial results for the first quarter of 2006, which showed a significant increase in Research & Development (R&D) spend, to 11.8 million euros. ...

  • 23.02.2006 – 08:20

    Zeltia: Report at 31 December 2005

    Madrid (ots/PRNewswire) - Group: - Capital increase at Zeltia. The placement of 10.75 million new shares among qualified international investors raised 65 million euro - R&D expenditure up 24% - Net revenues in 2005: 72 million euro - Net cash position at 31 December 2005: 93 million euro net of short-term financial debt and 51 million euro net of total financial debt PharmaMar: - Yondelis(R): - Phase III pivotal trial on ovarian cancer ...

  • 31.01.2006 – 08:30

    FDA Grants IND for PharmaMar's ZALYPSIS(r) to Enter Phase I Clinical Trials in US

    Madrid, Spain (ots/PRNewswire) - PharmaMar announced today that its Investigational New Drug application (IND)[1] has been accepted by the US Food and Drug Administration (FDA) for the clinical testing of Zalypsis(R) (PM00104/50), PharmaMar's novel marine anti-tumour agent. Zalypsis is already in Phase I clinical development in Europe, where three multicenter ...

  • 20.12.2005 – 08:25

    PharmaMar Confirms Intention to Submit MAA to EMEA for YONDELIS(R) in Soft Tissue Sarcoma

    Madrid (ots/PRNewswire) - - IDMC Recommends Adoption of 24hr Dosing in Pivotal Trial PharmaMar today announces that the independent data monitoring committee (IDMC) for the pivotal trial of YONDELIS(R) in Soft Tissue Sarcoma (STS) has reviewed data from a pre-planned interim analysis of the primary end-point, Time to Progression (TTP), which indicate that ...

  • 15.09.2005 – 08:30

    Aplidin(R) Commences Combination Trials

    Madrid (ots/PRNewswire) - - Further Steps in the Development of Aplidin(R) in Melanoma in First Line Therapy PharmaMar announces the initiation of a programme of combination studies with Aplidin(R) (plitidepsin), PharmaMar's novel marine-derived anti-tumour agent, originally isolated from the tunicate Aplidium albicans. Aplidin(R) in Combination with Dacarbazine (DTIC) The first study is a Phase I/II ...

  • 28.07.2005 – 10:11

    Zeltia S.A.: Report at 30 June 2005

    Madrid (ots/PRNewswire) - PharmaMar: - Orphan Drug designation granted by the FDA to Yondelis for the treatment of ovarian cancer in April. - Patient recruitment ongoing for the Phase III trial of Yondelis in ovarian cancer. - Promising results of Phase II trial of Yondelis in prostate cancer released at ASCO. - PharmaMar received 1 million dollars for complying with a milestone under the licensing and ...

  • 28.04.2005 – 09:44

    Zeltia Group: Report at 31 March 2005

    Madrid (ots/PRNewswire) - PharmaMar: - Zalypsis: this is PharmaMar's fifth compound to reach clinical development. - Aplidin: commenced Phase II studies on prostate and bladder cancer. - Yondelis: pivotal Phase III studies commenced on ovarian cancer patients. NeuroPharma: - Presented pre-clinical data at the 7th International Conference on Alzheimer's and Parkinson's Disease. Other: - ...

  • 18.04.2005 – 08:37

    PharmaMar Presents 13 Posters at AACR Highlighting Clinical and Preclinical Development Pipeline

    Anaheim, California (ots/PRNewswire) - PharmaMar today announces the presentation of thirteen posters highlighting advances with its clinical and preclinical compounds at the 96th Annual Meeting of the American Association for Cancer Research (AACR), taking place in Anaheim, California from 16-20 April 2005. The posters include results from research on Yondelis(R), ...

  • 24.02.2005 – 08:15

    Zeltia: Report at 31 December 2004

    Madrid, Spain (ots/PRNewswire) - PharmaMar: - Yondelis: - Due to the good results presented at the ASCO (American Society of Clinical Oncology) meeting, the randomised pivotal trial on soft-tissue sarcoma was expanded so as to compile a dossier for a regulatory application. - Results presented on ovarian cancer formed the basis for preparing Phase III trials in combination with Doxil. - The FDA (Food and Drug Administration) granted orphan ...

  • 17.02.2005 – 09:26

    Aplidin(R) Commences Phase II Clinical Trials in Prostate and Bladder Cancers

    Madrid, Spain (ots/PRNewswire) - PharmaMar announces that its second most advanced marine-derived anti-tumour agent, Aplidin(R), has commenced Phase II clinical trials in both prostate and bladder cancers. Phase II trial in Prostate Cancer This is the first trial of Aplidin in solid tumours to be carried out in the United States (US). This study will focus ...

  • 02.11.2004 – 10:52

    PharmaMar Reports New Data at ESMO Congress

    Vienna, Austria, November 2 (ots/PRNewswire) - - Significant Advances in the Clinical Development of Yondelis(TM) and Aplidin(R) PharmaMar, the biopharmaceutical company specialising in cancer therapy, presented new data from its two lead drugs, Yondelis(TM) and Aplidin(R), at the 29th European Society for Medical Oncology Congress (ESMO) held in Vienna, Austria from 29 October to 2 November 2004. Data ...

  • 28.10.2004 – 08:18

    PharmaMar's Kahalalide F, Phase II Trials for the Treatment of Severe Psoriasis

    Madrid (ots/PRNewswire) - PharmaMar today announced that Kahalalide F (KF), its marine-origin compound, has entered into Phase II trials for the treatment of patients with severe psoriasis. KF is currently undergoing Phase II clinical trials in various tumours: melanoma, non-small lung cancer and hepatocarcinoma. During the Phase I clinical trials on ...

  • 28.10.2004 – 08:16

    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 ...

  • 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 ...