ES2527544T1 - Tratamiento mono (PSI-7977) o de combinación con AAD para su uso en el tratamiento del VHC - Google Patents

Tratamiento mono (PSI-7977) o de combinación con AAD para su uso en el tratamiento del VHC Download PDF

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Publication number
ES2527544T1
ES2527544T1 ES12189195.6T ES12189195T ES2527544T1 ES 2527544 T1 ES2527544 T1 ES 2527544T1 ES 12189195 T ES12189195 T ES 12189195T ES 2527544 T1 ES2527544 T1 ES 2527544T1
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treatment
combination
psi
infected
compound
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Inventor
Barry M. Bernstein
Rajeev M. Menon
Amit Khatri
Sven MENSING
Sandeep Dutta
Daniel E. Cohen
Thomas Podsadecki
Scott C. Brun
Walid M. Awni
Emily O. Dumas
Cheri E. Klein
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AbbVie Inc
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AbbVie Inc
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Application filed by AbbVie Inc filed Critical AbbVie Inc
Publication of ES2527544T1 publication Critical patent/ES2527544T1/es
Pending legal-status Critical Current

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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401Proline; Derivatives thereof, e.g. captopril
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/41961,2,4-Triazoles
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    • A61K31/425Thiazoles
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/473Quinolines; Isoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/7042Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • A61K31/7072Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Abstract

Una combinación de al menos dos agentes antivirales de acción directa (AAD) para su uso en el tratamiento del VHC, donde dicho tratamiento no incluye la administración de interferón o ribavirina y dicho tratamiento dura 8, 9, 10, 11 o 12 semanas.

Claims (15)

  1. imagen1
  2. 3.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden BMS-790052 y BMS-650032. 10
  3. 4. La combinación de la reivindicación 3, donde dicho tratamiento es para un paciente no tratado previamente que está infectado con el genotipo 1 del VHC.
  4. 5.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden PSI-7977 y TMC-435. 15
  5. 6. La combinación de la reivindicación 5, donde dicho tratamiento es para un paciente no tratado previamente que está infectado con el genotipo 1 del VHC.
  6. 7.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden PSI-7977 y daclatasvir. 20
  7. 8. La combinación de la reivindicación 7, donde dicho tratamiento es para un paciente no tratado previamente que está infectado por el genotipo 1 del VHC.
  8. 9.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden PSI-7977 y GS-5885. 25
  9. 10.
    La combinación de la reivindicación 9, donde dicho tratamiento es para un paciente no tratado previamente que está infectado por el genotipo 1 del VHC.
  10. 11.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden:
    30 el compuesto 1 o una sal farmacéuticamente aceptable del mismo, y el compuesto 4 o una sal farmacéuticamente aceptable del mismo,
    donde el Compuesto 1 o la sal del mismo se coadministra con ritonavir. 35
  11. 12.
    La combinación de la reivindicación 11, donde dicho tratamiento es para un paciente no tratado previamente que está infectado por el genotipo 1 del VHC.
  12. 13.
    La combinación de la reivindicación 2, donde dichos al menos dos AAD comprenden:
    40 el compuesto 1 o una sal farmacéuticamente aceptable del mismo, el compuesto 2 o una sal farmacéuticamente aceptable del mismo, y el compuesto 4 o una sal farmacéuticamente aceptable del mismo,
    45 donde el Compuesto 1 o la sal del mismo se coadministra con ritonavir.
  13. 14. La combinación de la reivindicación 13, donde dicho tratamiento es para un paciente no tratado previamente que está infectado por el genotipo 1 del VHC.
    50 15. La combinación de la reivindicación 13, donde dicho tratamiento es para un no respondedor al interferón que está infectado por el genotipo 1 del VHC.
  14. 16. PSI-7977 para su uso en el tratamiento del VHC, donde dicho tratamiento no incluye la administración de
    interferón o ribavirina y dicho tratamiento dura 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23 o 24 55 semanas.
  15. 17. PSI-799 de la reivindicación 16, donde dicho tratamiento dura 12 semanas.
    2
ES12189195.6T 2011-10-21 2012-10-19 Tratamiento mono (PSI-7977) o de combinación con AAD para su uso en el tratamiento del VHC Pending ES2527544T1 (es)

Applications Claiming Priority (14)

Application Number Priority Date Filing Date Title
US201161550360P 2011-10-21 2011-10-21
US201161550360P 2011-10-21
US201161562176P 2011-11-21 2011-11-21
US201161562176P 2011-11-21
US201261587197P 2012-01-17 2012-01-17
US201261587197P 2012-01-17
US201261600468P 2012-02-17 2012-02-17
US201261600468P 2012-02-17
US201261619883P 2012-04-03 2012-04-03
US201261619883P 2012-04-03
US201261656253P 2012-06-06 2012-06-06
US201261656253P 2012-06-06
US201261711793P 2012-10-10 2012-10-10
US201261711793P 2012-10-10

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ES2527544T1 true ES2527544T1 (es) 2015-01-26

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US (2) US8809265B2 (es)
EP (1) EP2583680A3 (es)
JP (2) JP5677646B2 (es)
CN (2) CN104436197A (es)
AR (1) AR088408A1 (es)
AU (1) AU2013201532B2 (es)
BR (1) BR112014005617A2 (es)
CA (1) CA2811250C (es)
CH (1) CH707030B1 (es)
CL (2) CL2014000778A1 (es)
DE (6) DE202012013117U1 (es)
DK (1) DK2583680T1 (es)
DO (1) DOP2014000067A (es)
EA (1) EA201490836A1 (es)
ES (1) ES2527544T1 (es)
GB (4) GB2515942A (es)
HK (2) HK1199817A1 (es)
IL (1) IL230862A0 (es)
MX (1) MX2014004729A (es)
PH (1) PH12014502847A1 (es)
PT (2) PT107924A (es)
SE (2) SE1450020A1 (es)
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UY (1) UY34401A (es)
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ZA (1) ZA201406352B (es)

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NZ623396A (en) 2011-09-16 2016-07-29 Gilead Pharmasset Llc Methods for treating hcv
US8492386B2 (en) 2011-10-21 2013-07-23 Abbvie Inc. Methods for treating HCV
AU2013201532B2 (en) * 2011-10-21 2014-10-02 Abbvie Ireland Unlimited Company Methods for treating HCV
US8466159B2 (en) 2011-10-21 2013-06-18 Abbvie Inc. Methods for treating HCV
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