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    • 93. 发明专利
    • TREATMENT OF CHOLANGIOCARCINOMA WITH TPCS-2A INDUCED PHOTOCHEMICAL INTERNALISATION OF GEMCITABINE
    • SG11201903057XA
    • 2019-05-30
    • SG11201903057X
    • 2017-10-13
    • PCI BIOTECH AS
    • HØGSET ANDERSWALDAY PER EDVARDSELBO PÅL KRISTIANEIVINDVIK KRISTINFINNESAND LENA
    • A61K31/409A61K31/7068A61K33/24A61K41/00A61P35/00
    • INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 19 April 2018 (19.04.2018) WIP0 1 PCT omit n OH 10 0 0111 INIM Ell MIME 011 (10) International Publication Number WO 2018/069536 Al (51) International Patent Classification: A61K 31/409 (2006.01) A61K 41/00 (2006.01) A61K 31/7068 (2006.01) A61P 35/00 (2006.01) A61K 33/24 (2006.01) (21) International Application Number: Published: — with international search report (Art. 21(3)) PCT/EP2017/076257 (22) International Filing Date: 13 October 2017 (13.10.2017) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 1617526.7 14 October 2016 (14.10.2016) GB 1704719.2 24 March 2017 (24.03.2017) GB (71) Applicant: PCI BIOTECH AS [NO/NO]; Ullern- chausseen 64, 0379 Oslo (NO). (72) Inventors: HOGSET, Anders; Rognerudveien 55, N-0681 Oslo (NO). WALDAY, Per Edvard; Drammensveien 104D, N-0273 Oslo (NO). SELBO, Pal Kristian; Anne Manes vei 9, N-0373 Oslo (NO). EIVINDVIK, Kristin; Lilleruts vei 41, N-1364 Fornebu (NO). FINNESAND, Lena; Solligrenda 22, N-0491 Oslo (NO). = (74) Agent: JONES, Elizabeth Louise; Dehns, St Bride's House, 10 Salisbury Square, London Greater London EC4Y 8JD (GB). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, 1-1 MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). co (54) Title: TREATMENT OF CHOLANGIOCARCINOMA WITH TPCS-2A INDUCED PHOTOCHEMICAL INTERNALISATION OF GEMCITABINE \" (57) : The present invention provides TPCS2 a , gemcitabine and optionally another cytotoxic agent, preferably cisplatin, for C use in a method of treating a cholangiocarcinoma in a human patient comprising a photochemical internalization method. Related kits for performing the invention are also provided.
    • 100. 发明专利
    • Antigen delivery device and method
    • GB2517707A
    • 2015-03-04
    • GB201315288
    • 2013-08-28
    • PCI BIOTECH AS
    • GSET ANDERS HWALDAY PER EDVARDEIVINDVIK KRISTIN
    • A61N5/06
    • A device 1 for activating light-induced rupture of endocytic vesicles in target cells of a patent so as to effect delivery of an administered antigen to cytosol in the target cells, the device 1 being adapted to be worn by a patient over a region of the patients skin where an antigen and a photosensitising agent have been or are to be administered, wherein the device comprises: a rear surface that is configured to be worn against the patients skin, a retaining part e.g. strap 3a,b,c, for retaining the device 1 in place over the region of the patients skin during an activation cycle. A light source 13 arranged to illuminate the region of the patients skin from the rear surface of the device, a control system to control the operation of the light source after initiation of the activation cycle, and a power supply to power the light source and the control system. Wherein, the control system is configured to vary the output of the light source 13 with respect to time in accordance with a pre-configured output sequence, wherein the output sequence includes an initial stage where the output of the light source 13 is set to be zero or generally below that which could deliver a light dose that can activate light-induced rupture of endocytic vesicles to allow time for the antigen and photosensitising agent to reach the target cells, and a later stage where the output of the light source is set to deliver a light does which can activate the light-induced rupture of the endocytic vesicles for effecting the delivery of the administered antigen to the cytosol of the targeted cells.