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Fullmektig i Norge:
Org.nummer: 982702887
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Fullmektig i EP:
2018.04.03, US 201862652284 P
2018.04.11, US 201862656297 P
2018.04.13, US 201862657605 P
2018.10.05, US 201862741683 P
ANONYMOUS: "BLU-667 Targets RET-Altered Cancers.", vol. 8, no. 6, OF8, June 2018 (2018-06-01), pages 5pp, XP002792436, ISSN: 2159-8290, Retrieved from the Internet <URL:http://cancerdiscovery.aacrjournals.org/content/8/6/OF8.long> [retrieved on 20190625], DOI: 10.1158/2159-8290.CD-NB2018-050 (B1)
ANONYMOUS: "Estimating the Maximum Safe Starting Dose in Initial Clinical Trials for Therapeutics in Adult Healthy Volunteers", GUIDANCE FOR INDUSTRY, 1 July 2005 (2005-07-01), pages 1 - 30, XP093000005, Retrieved from the Internet <URL:https://www.fda.gov/media/72309/download> [retrieved on 20221121] (B1)
ANONYMOUS: "Phase 1 Study of the Highly-selective RET Inhibitor BLU-667 in Patients With Thyroid Cancer, Non-Small Cell Lung Cancer, and Other Advanced Solid Tumors", INTERNET CITATION, 21 April 2017 (2017-04-21), pages 8pp, XP002783685, Retrieved from the Internet <URL:https://www.clinicaltrials.gov/ct2/history/NCT03037385?V_3=View#StudyPageTop> [retrieved on 20180807] (B1)
BRUCE G. ROBINSON ET AL: "Vandetanib (100 mg) in Patients with Locally Advanced or Metastatic Hereditary Medullary Thyroid Cancer", JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM, vol. 95, no. 6, 1 June 2010 (2010-06-01), US, pages 2664 - 2671, XP055599340, ISSN: 0021-972X, DOI: 10.1210/jc.2009-2461 (B1)
KAMIL NOOR: "Dose estimation, conversion and translation from animal to human and human to animal for clinical and animal studies", INT. J. BIOL. BIOTECH., 1 July 2017 (2017-07-01), pages 311 - 317, XP093000013, Retrieved from the Internet <URL:https://www.researchgate.net/publication/322329638_Dose_estimation_conversion_and_translation_from_animal_to_human_and_human_to_animal_for_clinical_and_animal_studies> [retrieved on 20221121] (B1)
POUND PANDORA J ET AL: "Is it possible to overcome issues of external validity in preclinical animal research? Why most animal models are bound to fail", J. TRANSL MED, 1 January 2018 (2018-01-01), pages 1 - 8, XP093000231, Retrieved from the Internet <URL:https://www.researchgate.net/publication/328793141_Is_it_possible_to_overcome_issues_of_external_validity_in_preclinical_animal_research_Why_most_animal_models_are_bound_to_fail> [retrieved on 20221121], DOI: 10.1186/s12967-018-1678-1 (B1)
WO-A1-2018/213329 (B1)
SHANNON REAGAN-SHAW ET AL: "Dose translation from animal to human studies revisited", THE FASEB JOURNAL, vol. 22, no. 3, 1 March 2008 (2008-03-01), & EXPERIMENTAL BIOLOGY MEETING; SAN DIEGO, CA, USA; APRIL 21 -25, 2018, pages 659 - 661, XP055542714, ISSN: 0892-6638, DOI: 10.1096/fj.07-9574LSF (B1)
SUBBIAH ET AL.: "Abstract CT043: Highly potent and selective RET inhibitor, BLU-667, achieves proof of concept in a phase I study of advanced, RET-altered solid tumors", vol. 78, no. 13, Supplement 1, July 2018 (2018-07-01), Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL, XP002792435, ISSN: 1538-7445, Retrieved from the Internet <URL:http://cancerres.aacrjournals.org/content/78/13_Supplement/CT043> [retrieved on 20190626], DOI: 10.1158/1538-7445.AM2018-CT043 (B1)
SUBBIAH V. ET AL: "Clinical activity and safety of the RET inhibitor pralsetinib in patients with RET fusion-positive solid tumours: update from the ARROW trial", ASCO, 4 June 2021 (2021-06-04), pages 1 - 1, XP093000210, Retrieved from the Internet <URL:https://ascopubs.org/doi/abs/10.1200/JCO.2021.39.15_suppl.3079> [retrieved on 20221121] (B1)
VIVEK SUBBIAH ET AL: "Precision Targeted Therapy with BLU-667 for RET -Driven Cancers", CANCER DISCOVERY, vol. 8, no. 7, 15 April 2018 (2018-04-15), US, pages 836 - 849, XP055599279, ISSN: 2159-8274, DOI: 10.1158/2159-8290.CD-18-0338 (B1)
WO-A1-2017/079140 (B1)
WO-A1-2018/071447 (B1)
RAMI RAHAL ET AL: "BLU-667 is a potent and highly selective RET inhibitor being developed for RET- driven cancers", MOLECULAR CANCER THERAPEUTICS, 1 January 2018 (2018-01-01), pages 1, XP055644433, Retrieved from the Internet <URL:https://www.blueprintmedicines.com/wp-content/uploads/2018/12/BLU-667-EORTC-2017-BPM.pdf> [retrieved on 20191120] (B1)
Statushistorie
Hovedstatus | Beslutningsdato, detaljstatus |
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EP patent gjort gjeldende i Norge | EP patent besluttet gjeldende i Norge |
EP under behandling | Forespørsel om å gjøre EP patent gyldig er mottatt |
Korrespondanse
Dato
Type korrespondanse
Journal beskrivelse
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Innkommende
EP Publiseringsdokument fra EPO
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Innkommende
EP Publiseringsdokument fra EPO
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Innkommende
EP Publiseringsdokument fra EPO
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Innkommende
EP Publiseringsdokument fra EPO
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Utgående
EP Varsel om betaling av første årsavgift (3319) (PTEP3773589)
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Utgående
EP Registreringsbrev (3210) (PTEP3773589)
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Innkommende
Søknadsskjema Patent
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Innkommende
EP Publiseringsdokument fra EPO
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Til betaling:
Betalingshistorikk:
Beskrivelse / Fakturanummer | Betalingsdato | Beløp | Betaler | Status |
---|---|---|---|---|
Årsavgift 7. avg. år (EP) expand_more expand_less | 2025.04.09 | 2860,0 | CPA GLOBAL LIMITED | Betalt og godkjent |
Årsavgift 7. avg. år (EP)
2860,0 = 1 X 2860,0
En ordre på saken er opprettet av: Supplier Payments (08.04.2025 07:27:39): Betalt |
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Årsavgift 6. avg. år (EP) | 2024.04.09 | 2600 | CPA GLOBAL LIMITED | Betalt og godkjent |
32401457 expand_more expand_less | 2024.01.31 | 5500 | ZACCO NORWAY AS | Betalt |
Valideringsgebyr EP-patent
5500 = 1 X 5500
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