JP2004525889A5 - - Google Patents

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JP2004525889A5
JP2004525889A5 JP2002559408A JP2002559408A JP2004525889A5 JP 2004525889 A5 JP2004525889 A5 JP 2004525889A5 JP 2002559408 A JP2002559408 A JP 2002559408A JP 2002559408 A JP2002559408 A JP 2002559408A JP 2004525889 A5 JP2004525889 A5 JP 2004525889A5
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alkyl
dioxo
dioxoisoindoline
piperidyl
methyl
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Claims (13)

  1. 以下の式を有する化合物。
    Figure 2004525889
    [式中、
    R1はH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、C(O)R3、C(S)R3、C(O)OR4、(C1-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、C(O)NHR3、C(S)NHR3、C(O)NR3R3'、C(S)NR3R3'または(C1-C8)アルキル-O(CO)R5であり、
    R2はHまたは(C1-C8)アルキルであり、
    R3及びR3'は独立して(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であり、
    R4は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、(C1-C4)アルキル-OR5、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、または(C0-C4)アルキル-(C2-C5)ヘテロアリールであり、
    R5は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、または(C2-C5)ヘテロアリールであり、
    R6はそれぞれ独立してH、(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C2-C5)ヘテロアリール、または(C0-C8)アルキル-C(O)O-R5であるか、R6基が結合してヘテロシクロアルキル基を形成し、そして
    *はキラル炭素中心を示す。]
  2. R1がH、(C1-C4)アルキル、CH2OCH3、CH2CH2OCH3、または
    Figure 2004525889
    であり、QがOまたはSであり、そしてR7はそれぞれ独立してH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、ハロゲン、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であるか、あるいは隣り合ったR7が一緒になって二環式アルキル環またはアリール環を形成する、請求項1記載の化合物。
  3. R1がC(O)R3である、請求項1記載の化合物。
  4. R1がC(O)OR4である、請求項1記載の化合物。
  5. 以下の式を有する化合物。
    Figure 2004525889
    [式中、
    R1はH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、C(O)R3、C(S)R3、C(O)OR4、(C1-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、C(O)NHR3、C(S)NHR3、C(O)NR3R3'、C(S)NR3R3'または(C1-C8)アルキル-O(CO)R5であり、
    R2はHまたは(C1-C8)アルキルであり、
    R3及びR3'は独立して(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であり、
    R4は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、(C1-C4)アルキル-OR5、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、または(C0-C4)アルキル-(C2-C5)ヘテロアリールであり、
    R5は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、または(C2-C5)ヘテロアリールであり、
    R6はそれぞれ独立してH、(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C2-C5)ヘテロアリール、または(C0-C8)アルキル-C(O)O-R5であるか、R6基が結合してヘテロシクロアルキル基を形成し、そして
    *はキラル炭素中心を示す。]
  6. R1がH、(C1-C4)アルキル、CH2OCH3、CH2CH2OCH3、または
    Figure 2004525889
    であり、QがOまたはSであり、そしてR7はそれぞれ独立してH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、ハロゲン、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であるか、あるいは隣り合ったR7が一緒になって二環式アルキル環またはアリール環を形成する、請求項5記載の化合物。
  7. R1がC(O)R3である、請求項5記載の化合物。
  8. R1がC(O)OR4である、請求項5記載の化合物。
  9. 以下の式を有する化合物。
    Figure 2004525889
    [式中、
    R1はH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、C(O)R3、C(S)R3、C(O)OR4、(C1-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、C(O)NHR3、C(S)NHR3、C(O)NR3R3'、C(S)NR3R3'または(C1-C8)アルキル-O(CO)R5であり、
    R2はHまたは(C1-C8)アルキルであり、
    R3及びR3'は独立して(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であり、
    R4は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、(C1-C4)アルキル-OR5、ベンジル、アリール、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、または(C0-C4)アルキル-(C2-C5)ヘテロアリールであり、
    R5は(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、または(C2-C5)ヘテロアリールであり、
    R6はそれぞれ独立してH、(C1-C8)アルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、(C2-C5)ヘテロアリール、または(C0-C8)アルキル-C(O)O-R5であるか、R6基が結合してヘテロシクロアルキル基を形成し、そして
    *はキラル炭素中心を示す。]
  10. R1がH、(C1-C4)アルキル、CH2OCH3、CH2CH2OCH3、または
    Figure 2004525889
    であり、QがOまたはSであり、そしてR7はそれぞれ独立してH、(C1-C8)アルキル、(C3-C7)シクロアルキル、(C2-C8)アルケニル、(C2-C8)アルキニル、ベンジル、アリール、ハロゲン、(C0-C4)アルキル-(C1-C6)ヘテロシクロアルキル、(C0-C4)アルキル-(C2-C5)ヘテロアリール、(C0-C8)アルキル-N(R6)2、(C1-C8)アルキル-OR5、(C1-C8)アルキル-C(O)OR5、(C1-C8)アルキル-O(CO)R5、またはC(O)OR5であるか、あるいは隣り合ったR7が一緒になって二環式アルキル環またはアリール環を形成する、請求項9記載の化合物。
  11. R1がC(O)R3である、請求項9記載の化合物。
  12. R1がC(O)OR4である、請求項9記載の化合物。
  13. N-[2-(2,6-ジオキソ-ピペリジン-3-イル)-1,3-ジオキソ-2,3-ジヒドロ-1H-イソインドール-4-イルメチル]-アセトアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}シクロプロピル-カルボキシアミド;
    1-tert-ブチル-3-[2-(2,6-ジオキソ-ピペリジン-3-イル)-1,3-ジオキソ-2,3-ジヒドロ-1H-イソインドール-4-イルメチル]-尿素;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-3,3-ジメチルブタンアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}プロパンアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-3-ピリジルカルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}ヘプタンアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-2-フリルカルボキシアミド;
    2-アミノ-N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}アセトアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-2-チエニルカルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(エチルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}ブタンアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-2-ピリジルカルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}-2-メチルプロパンアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}シクロペンチルカルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}シクロヘキシルカルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(ブチルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(プロピルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(シクロヘキシルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}[(メチルエチルアミノ)]カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(オクチルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(シクロプロピルアミノ)カルボキシアミド;
    N-{[2-(2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチル}(ジエチルアミノ)カルボキシアミド;
    シクロプロピル-N-{2-(3-メチル-2,6-ジオキソ(3-ピペリジル))-1,3-ジオキソイソインドリン-4-イル]メチルカルボキシアミド;
    である請求項1記載の化合物。
JP2002559408A 2000-12-27 2001-12-21 イソインドール−イミド化合物、組成物、およびそれらの使用 Expired - Fee Related JP4284071B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US25837200P 2000-12-27 2000-12-27
US09/972,487 US20030045552A1 (en) 2000-12-27 2001-10-05 Isoindole-imide compounds, compositions, and uses thereof
PCT/US2001/050401 WO2002059106A1 (en) 2000-12-27 2001-12-21 Isoindole-imide compounds, compositions, and uses thereof

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JP2004525889A JP2004525889A (ja) 2004-08-26
JP2004525889A5 true JP2004525889A5 (ja) 2006-01-05
JP4284071B2 JP4284071B2 (ja) 2009-06-24

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JP2005321049A Expired - Fee Related JP4648822B2 (ja) 2000-12-27 2005-11-04 イソインドール−イミド化合物、組成物、およびそれらの使用
JP2010110388A Pending JP2010195824A (ja) 2000-12-27 2010-05-12 イソインドール−イミド化合物、組成物、およびそれらの使用

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US (1) US20030045552A1 (ja)
EP (3) EP2168958A1 (ja)
JP (3) JP4284071B2 (ja)
KR (4) KR100802713B1 (ja)
AT (1) ATE352548T1 (ja)
AU (3) AU2002248252B2 (ja)
CA (1) CA2433021C (ja)
CY (1) CY1106423T1 (ja)
CZ (1) CZ20032041A3 (ja)
DE (1) DE60126344T2 (ja)
DK (1) DK1363900T3 (ja)
ES (1) ES2275758T3 (ja)
HK (1) HK1061396A1 (ja)
HU (1) HU229003B1 (ja)
IL (2) IL156646A0 (ja)
MX (1) MXPA03005786A (ja)
NZ (1) NZ526893A (ja)
PT (1) PT1363900E (ja)
WO (1) WO2002059106A1 (ja)
ZA (1) ZA200305759B (ja)

Families Citing this family (227)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6228879B1 (en) * 1997-10-16 2001-05-08 The Children's Medical Center Methods and compositions for inhibition of angiogenesis
US6429221B1 (en) 1994-12-30 2002-08-06 Celgene Corporation Substituted imides
HU228769B1 (en) * 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
US5635517B1 (en) * 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
US7629360B2 (en) * 1999-05-07 2009-12-08 Celgene Corporation Methods for the treatment of cachexia and graft v. host disease
US6458810B1 (en) 2000-11-14 2002-10-01 George Muller Pharmaceutically active isoindoline derivatives
DK1353672T3 (da) * 2000-11-30 2008-01-21 Childrens Medical Center Syntese af 4-amino-thalidomidenantiomerer
US20030045552A1 (en) * 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
DE10137163A1 (de) * 2001-07-30 2003-02-13 Bayer Ag Substituierte Isoindole und ihre Verwendung
ATE428419T1 (de) * 2001-08-06 2009-05-15 Childrens Medical Center Antiangiogenese wirkung von stickstoffsubstituierten thalidomid-analoga
AU2003211941A1 (en) * 2002-02-14 2003-09-04 Ajinomoto Co., Inc. Method of analyzing aminofunctional compound and analytical reagent
US7498171B2 (en) 2002-04-12 2009-03-03 Anthrogenesis Corporation Modulation of stem and progenitor cell differentiation, assays, and uses thereof
WO2003086373A1 (en) * 2002-04-12 2003-10-23 Celgene Corporation Methods for identification of modulators of angiogenesis, compounds discovered thereby, and methods of treatment using the compounds
USRE48890E1 (en) 2002-05-17 2022-01-11 Celgene Corporation Methods for treating multiple myeloma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione after stem cell transplantation
US7323479B2 (en) * 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
AU2006202316B2 (en) * 2002-05-17 2008-04-10 Celgene Corporation Methods and compositions using immunomodulatory compounds for treatment and management of cancers and other diseases
MXPA04011311A (es) 2002-05-17 2005-02-14 Celgene Corp Metodos y composiciones que utilizan compuestos inmunomoduladores para el tratamiento y el manejo de canceres y otras enfermedades.
US7393862B2 (en) * 2002-05-17 2008-07-01 Celgene Corporation Method using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for treatment of certain leukemias
US7968569B2 (en) * 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
EP1900369A1 (en) 2002-10-15 2008-03-19 Celgene Corporation Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of myelodysplastic syndromes
US8404716B2 (en) 2002-10-15 2013-03-26 Celgene Corporation Methods of treating myelodysplastic syndromes with a combination therapy using lenalidomide and azacitidine
US11116782B2 (en) 2002-10-15 2021-09-14 Celgene Corporation Methods of treating myelodysplastic syndromes with a combination therapy using lenalidomide and azacitidine
US7189740B2 (en) * 2002-10-15 2007-03-13 Celgene Corporation Methods of using 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myelodysplastic syndromes
US8404717B2 (en) * 2002-10-15 2013-03-26 Celgene Corporation Methods of treating myelodysplastic syndromes using lenalidomide
AU2003286663B2 (en) * 2002-10-24 2009-08-13 Celgene Corporation Methods of using and compositions comprising immunomodulatory compounds for treatment, modification and management of pain
US20050203142A1 (en) * 2002-10-24 2005-09-15 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment, modification and management of pain
US8034831B2 (en) 2002-11-06 2011-10-11 Celgene Corporation Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies
US7563810B2 (en) * 2002-11-06 2009-07-21 Celgene Corporation Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases
US20040171147A1 (en) * 2002-11-26 2004-09-02 Hariri Robert J. Cytotherapeutics, cytotherapeutic units and methods for treatments using them
JP4613157B2 (ja) * 2003-01-14 2011-01-12 サイトキネティクス・インコーポレーテッド 化合物、組成物および方法
AU2004212009B2 (en) * 2003-02-13 2010-07-29 Celularity Inc. Use of umbilical cord blood to treat individuals having a disease, disorder or condition
US7320992B2 (en) * 2003-08-25 2008-01-22 Amgen Inc. Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use
UA83504C2 (en) * 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
CN1867331B (zh) * 2003-09-17 2010-05-26 美国政府健康及人类服务部 作为TNF-α调节剂的沙利度胺类似物
US8952895B2 (en) 2011-06-03 2015-02-10 Apple Inc. Motion-based device operations
US7612096B2 (en) * 2003-10-23 2009-11-03 Celgene Corporation Methods for treatment, modification and management of radiculopathy using 1-oxo-2-(2,6-dioxopiperidin-3yl)-4-aminoisoindoline
OA13284A (en) * 2003-11-06 2007-01-31 Corporation Celgene Methods and compositions using thalidomide for thetreatment and management of cancers and other dis eases.
US20050100529A1 (en) * 2003-11-06 2005-05-12 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of asbestos-related diseases and disorders
AU2004296765B2 (en) * 2003-12-02 2011-03-24 Celgene Corporation Methods and compositions for the treatment and management of hemoglobinopathy and anemia
US20050143344A1 (en) * 2003-12-30 2005-06-30 Zeldis Jerome B. Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases
AU2005226649B2 (en) 2004-03-22 2010-04-29 Celgene Corporation Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of skin diseases or disorders
US20050222209A1 (en) * 2004-04-01 2005-10-06 Zeldis Jerome B Methods and compositions for the treatment, prevention or management of dysfunctional sleep and dysfunctional sleep associated with disease
BRPI0418742A (pt) * 2004-04-14 2007-09-11 Celgene Corp métodos de tratamento, prevenção ou controle de uma sìndrome mielodisplásica, de redução ou evitação de um efeito adverso associado com a administração de um segundo ingrediente ativo em um paciente sofrendo de um sìndrome mielodisplásica, composição farmacêutica, forma de dosagem unitária única, e, kit
MXPA06012278A (es) * 2004-04-23 2007-01-31 Celgene Corp Metodos de uso y composiciones que comprenden compuestos inmunomoduladores para el tratamiento y manejo de la hipertension pulmonar.
JP2005336157A (ja) * 2004-04-30 2005-12-08 Arigen Inc 光学活性サリドマイドおよびその誘導体の製造法
JP2007536223A (ja) * 2004-05-05 2007-12-13 セルジーン・コーポレーション 骨髄増殖性疾患の治療及び管理のための免疫調節化合物を含む組成物、及びその使用方法
EP1765327B1 (en) 2004-06-17 2014-08-13 Cytokinetics, Inc. Compounds, compositions and methods
US7176222B2 (en) 2004-07-27 2007-02-13 Cytokinetics, Inc. Syntheses of ureas
EP2479172B1 (en) * 2004-09-03 2013-10-09 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines
MX2007005040A (es) * 2004-10-28 2007-06-19 Celgene Corp Metodos y composiciones usando moduladores de pde4 para el tratamiento y manejo de lesion al sistema nervioso central.
AU2005304420A1 (en) * 2004-11-12 2006-05-18 Celgene Corporation Methods and compositions using immunomodulatory compounds for treatment and management of parasitic diseases
CA2588597A1 (en) * 2004-11-23 2006-06-01 Celgene Corporation Methods and compositions using immunomodulatory compounds for treatment and management of central nervous system injury
US20060270707A1 (en) * 2005-05-24 2006-11-30 Zeldis Jerome B Methods and compositions using 4-[(cyclopropanecarbonylamino)methyl]-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione for the treatment or prevention of cutaneous lupus
JP2008544818A (ja) * 2005-06-30 2008-12-11 アントフロゲネシス コーポレーション 胎盤由来コラーゲンバイオ線維を用いた鼓膜の修復
ES2430545T3 (es) 2005-06-30 2013-11-21 Celgene Corporation Procedimientos para la preparación de compuestos de 4-amino-2-(2,6-dioxopiperidin-3-il)isoindolina-1,3-diona
WO2007009061A2 (en) * 2005-07-13 2007-01-18 Anthrogenesis Corporation Ocular plug formed from placenta derived collagen biofabric
EP1919500A2 (en) * 2005-07-13 2008-05-14 Anthrogenesis Corporation Treatment of leg ulcers using placenta derived collagen biofabric
US7538223B2 (en) 2005-08-04 2009-05-26 Cytokinetics, Inc. Compounds, compositions and methods
ES2434946T3 (es) * 2005-08-31 2013-12-18 Celgene Corporation Compuestos de isoindol imida y composiciones que los comprenden y métodos para usarlo
CA2621136C (en) * 2005-09-01 2014-10-14 Celgene Corporation Immunological uses of immunomodulatory compounds for vaccine and anti-infectious disease therapy
US20070066512A1 (en) * 2005-09-12 2007-03-22 Dominique Verhelle Methods and compositions using immunomodulatory compounds for the treatment of disorders associated with low plasma leptin levels
CN1939922B (zh) * 2005-09-27 2010-10-13 天津和美生物技术有限公司 可抑制细胞释放肿瘤坏死因子的5H-噻吩[3,4-c]吡咯-4,6-二酮衍生物
WO2007047468A2 (en) 2005-10-13 2007-04-26 Anthrogenesis Corporation Immunomodulation using placental stem cells
US20070208000A1 (en) * 2005-12-15 2007-09-06 Morgan Bradley P Certain chemical entities, compositions and methods
US7825120B2 (en) * 2005-12-15 2010-11-02 Cytokinetics, Inc. Certain substituted ((piperazin-1-ylmethyl)benzyl)ureas
AR058347A1 (es) * 2005-12-15 2008-01-30 Cytokinetics Inc Entidades quimias composiciones y metodos
US20070197505A1 (en) * 2005-12-15 2007-08-23 Morgan Bradley P Certain chemical entities, compositions and methods
US7718657B2 (en) 2005-12-16 2010-05-18 Cytokinetics, Inc. Certain indanyl urea modulators of the cardiac sarcomere
WO2007078839A2 (en) * 2005-12-19 2007-07-12 Cytokinetics, Inc. Compounds, compositions and methods
CN101374941A (zh) 2005-12-29 2009-02-25 人类起源公司 采集和保存胎盘干细胞的改良组合物及其使用方法
KR20190104428A (ko) 2005-12-29 2019-09-09 안트로제네시스 코포레이션 태반 줄기 세포 집단
US20070155791A1 (en) * 2005-12-29 2007-07-05 Zeldis Jerome B Methods for treating cutaneous lupus using aminoisoindoline compounds
US8247582B2 (en) * 2006-02-07 2012-08-21 Battelle Memorial Institute Esters of 5-hydroxymethylfurfural and methods for their preparation
US20080064876A1 (en) * 2006-05-16 2008-03-13 Muller George W Process for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
TW200806625A (en) * 2006-05-26 2008-02-01 Astrazeneca Ab Therapeutic compounds
WO2008001115A2 (en) * 2006-06-29 2008-01-03 Astex Therapeutics Limited Pharmaceutical combinations of 1-cyclopropyl-3- [3- (5-m0rphoolin-4-ylmethyl-1h-benzoimidazol-2-yl) -lh-1-pyrazol- 4-yl] -urea
CL2007002218A1 (es) * 2006-08-03 2008-03-14 Celgene Corp Soc Organizada Ba Uso de 3-(4-amino-1-oxo-1,3-dihidro-isoindol-2-il)-piperidina 2,6-diona para la preparacion de un medicamento util para el tratamiento de linfoma de celula de capa.
US7993918B2 (en) 2006-08-04 2011-08-09 Anthrogenesis Corporation Tumor suppression using placental stem cells
WO2008021391A1 (en) * 2006-08-15 2008-02-21 Anthrogenesis Corporation Umbilical cord biomaterial for medical use
RU2448101C2 (ru) * 2006-08-30 2012-04-20 Селджин Корпорейшн 5-замещенные изоиндолиновые соединения
US8877780B2 (en) * 2006-08-30 2014-11-04 Celgene Corporation 5-substituted isoindoline compounds
CA2660806C (en) * 2006-08-30 2015-06-16 Celgene Corporation 5-substituted isoindoline compounds
JP5567339B2 (ja) * 2006-09-15 2014-08-06 セルジーン コーポレイション N−メチルアミノメチルイソインドール化合物、それを含む組成物、及びその使用方法
WO2008042441A1 (en) * 2006-10-03 2008-04-10 Anthrogenesis Corporation Use of umbilical cord biomaterial for ocular surgery
WO2008060377A2 (en) 2006-10-04 2008-05-22 Anthrogenesis Corporation Placental or umbilical cord tissue compositions
JP5769925B2 (ja) 2006-10-06 2015-08-26 アントフロゲネシス コーポレーション ヒト胎盤コラーゲン組成物、並びにそれらの製造方法及び使用方法
MX349225B (es) * 2007-02-12 2017-07-19 Anthrogenesis Corp Uso de celulas madre placentarias para preparar medicamentos utiles en el tratamiento de padecimientos inflamatorios.
CA2677679A1 (en) * 2007-02-12 2008-08-21 Anthrogenesis Corporation Hepatocytes and chondrocytes from adherent placental stem cells; and cd34+, cd45- placental stem cell-enriched cell populations
KR20090121400A (ko) * 2007-03-20 2009-11-25 셀진 코포레이션 4'-o-치환된 아이소인돌린 유도체 및 이를 포함하는 조성물 및 이의 사용 방법
US20100172830A1 (en) * 2007-03-29 2010-07-08 Cellx Inc. Extraembryonic Tissue cells and method of use thereof
WO2009020590A1 (en) * 2007-08-07 2009-02-12 Celgene Corporation Methods for treating lymphomas in certain patient populations and screening patients for said therapy
MX2010003217A (es) * 2007-09-26 2010-07-30 Celgene Cellular Therapeutics Celulas angiogenicas de perfundido de placenta humana.
MY157495A (en) 2007-09-26 2016-06-15 Celgene Corp 6-,7-, or 8-substituted quinazolinone derivatives and compositions comprising and methods of using the same
KR20210022148A (ko) 2007-09-28 2021-03-02 안트로제네시스 코포레이션 인간 태반 관류액 및 인간 태반-유래 중간체 천연 킬러 세포를 사용한 종양 억제 방법
US20090136471A1 (en) * 2007-11-07 2009-05-28 Anthrogenesis Corporation Treatment of premature birth complications
WO2009061445A2 (en) * 2007-11-08 2009-05-14 Celgene Corporation Use of immunomodulatory compounds for the treatment of disorders associated with endothelial dysfunction
US20090155207A1 (en) * 2007-11-29 2009-06-18 Hariri Robert J Use of Immunomodulatory Compounds for the Treatment of Transverse Myelitis, Multiple Sclerosis, and Other Disorders
WO2009085234A2 (en) * 2007-12-20 2009-07-09 Signal Pharmaceuticals, Inc. Use of micro-rna as a biomarker of immunomodulatory drug activity
EP2249835A1 (en) * 2008-01-29 2010-11-17 Celgene Corporation Methods using immunomodulatory compounds for modulating level of cd59
WO2009105256A2 (en) * 2008-02-20 2009-08-27 Celgene Corporation Method of treating cancer by administering an immunomodulatory compound in combination with a cd40 antibody or cd40 ligand
MX2011001991A (es) * 2008-08-20 2011-03-29 Anthrogenesis Corp Tratamiento de la apoplejia utilizando celulas placentarias aisladas.
EP3539380A3 (en) * 2008-08-20 2019-12-18 Celularity, Inc. Improved cell composition and methods of making the same
WO2010021756A1 (en) * 2008-08-22 2010-02-25 Anthrogenesis Corporation Methods and compositions for treatment of bone defects with placental cell populations
KR101696938B1 (ko) * 2008-10-29 2017-01-16 셀진 코포레이션 암의 치료에 사용하기 위한 이소인돌린 화합물
DK2367932T3 (da) * 2008-11-19 2019-09-23 Celularity Inc Amnion-afledte adhærente celler
ES2731340T3 (es) * 2008-11-21 2019-11-15 Celularity Inc Tratamiento de enfermedades, trastornos o afecciones pulmonares utilizando células placentarias
WO2010077686A1 (en) * 2008-12-08 2010-07-08 Sirtris Pharmaceuticals, Inc. Isoindolinone and related analogs as sirtuin modulators
RU2742171C2 (ru) 2009-03-25 2021-02-02 Антродженезис Корпорейшн Супрессия опухолей с использованием полученных из плаценты человека промежуточных естественных киллерных клеток и иммуномодулирующих соединений
JP5645816B2 (ja) 2009-05-25 2014-12-24 国立大学法人東京工業大学 中枢神経細胞の増殖及び分化に係る中核因子を含む医薬組成物
CN101580501B (zh) 2009-06-01 2011-03-09 南京卡文迪许生物工程技术有限公司 3-(取代二氢异吲哚酮-2-基)-2,6-哌啶二酮的合成方法及其中间体
CA2786266A1 (en) 2010-01-05 2011-07-14 Celgene Corporation A combination of an immunomodulatory compound and an artemisinin or a derivative thereof for treating cancer
ES2646750T3 (es) * 2010-01-26 2017-12-15 Anthrogenesis Corporation Tratamiento de cánceres relacionados con hueso utilizando células madre placentarias
SI3202461T1 (sl) * 2010-02-11 2019-05-31 Celgene Corporation Derivati arilmetoksi izoindolina in sestavki, ki jih vsebujejo in metode uporabe le teh
HUE029144T2 (hu) 2010-04-07 2017-02-28 Anthrogenesis Corp Angiogenezis méhlepény õssejtek használatával
MX341050B (es) 2010-04-07 2016-08-05 Celgene Corp * Metodos para tratar infeccion viral respiratoria.
CA2795401A1 (en) 2010-04-08 2011-10-13 Anthrogenesis Corporation Treatment of sarcoidosis using placental stem cells
EP2593542B1 (en) 2010-07-13 2018-01-03 Anthrogenesis Corporation Methods of generating natural killer cells
US20140031325A1 (en) 2010-12-06 2014-01-30 Celgene Corporation Combination therapy with lenalidomide and a cdk inhibitor for treating multiple myeloma
WO2012092485A1 (en) 2010-12-31 2012-07-05 Anthrogenesis Corporation Enhancement of placental stem cell potency using modulatory rna molecules
DK2683708T3 (da) 2011-03-11 2018-01-29 Celgene Corp Faste former af 3-(5-amino-2-methyl-4-oxo-4h-quinazolin-3-yl)-piperidin-2,6-dion og farmaceutiske sammensætninger og anvendelser deraf
WO2012135299A1 (en) 2011-03-28 2012-10-04 Deuteria Pharmaceuticals Inc 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
JP2014517915A (ja) 2011-04-18 2014-07-24 セルジーン コーポレイション 多発性骨髄腫治療のためのバイオマーカー
MX353482B (es) 2011-04-29 2018-01-16 Celgene Corp Metodos para el tratamiento del cancer y enfermedades inflamatorias utilizando cereblon como predictor.
EP3443968A1 (en) 2011-06-01 2019-02-20 Celularity, Inc. Treatment of pain using placental stem cells
US8927725B2 (en) 2011-12-02 2015-01-06 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Thio compounds
EP3967323A3 (en) 2012-06-06 2022-05-04 Bionor Immuno AS Hiv vaccine
CA3136093A1 (en) 2012-06-29 2014-01-03 Celgene Corporation Methods for determining drug efficacy using cereblon-associated proteins
US9587281B2 (en) 2012-08-14 2017-03-07 Celgene Corporation Cereblon isoforms and their use as biomarkers for therapeutic treatment
AU2013204922B2 (en) 2012-12-20 2015-05-14 Celgene Corporation Chimeric antigen receptors
EP2943201B2 (en) 2013-01-14 2020-07-29 Deuterx, LLC 3-(5-substituted-4-oxoquinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
CN105142651A (zh) 2013-02-05 2015-12-09 人类起源公司 来自胎盘的自然杀伤细胞
WO2014152833A1 (en) 2013-03-14 2014-09-25 Deuterx, Llc 3-(substituted-4-oxo-quinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
EP2970372B1 (en) 2013-03-15 2020-09-30 Celgene Corporation Modified t lymphocytes
WO2015007337A1 (en) 2013-07-19 2015-01-22 Bionor Immuno As Method for the vaccination against hiv
CN103396397A (zh) * 2013-08-14 2013-11-20 中国人民解放军军事医学科学院毒物药物研究所 来那度胺衍生物及其作为药物的用途
CN103421061A (zh) * 2013-08-14 2013-12-04 中国药科大学 来那度胺衍生物、其制法及其医药用途
US9969687B2 (en) * 2013-12-23 2018-05-15 Norgine B.V. Compounds useful as CCR9 modulators
KR20170002446A (ko) * 2014-04-14 2017-01-06 아비나스 인코포레이티드 단백질분해의 이미드-기초된 조절인자 및 연관된 이용 방법
JP6640126B2 (ja) 2014-06-27 2020-02-05 セルジーン コーポレイション セレブロン及び他のe3ユビキチンリガーゼの立体構造の変化を誘導するための組成物及び方法
JP2017523166A (ja) 2014-07-11 2017-08-17 ビオノール イミュノ エーエスBionor Immuno As ヒト免疫不全ウイルスi(hiv)の病理学的影響を減少及び/若しくは遅延させるか又は後天性免疫不全症候群(aids)を発症するリスクを低減させる方法
SI3182996T1 (sl) 2014-08-22 2023-04-28 Celgene Corporation Postopki zdravljenja multiplega mieloma z imunomodulatornimi spojinami v kombinaciji s protitelesi
KR102191256B1 (ko) * 2014-10-30 2020-12-15 강푸 바이오파마슈티칼즈 리미티드 이소인돌린 유도체, 이의 중간체, 제조방법, 약물 조성물 및 응용
US9694084B2 (en) 2014-12-23 2017-07-04 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
CN107257800B (zh) 2014-12-23 2020-06-30 达纳-法伯癌症研究所股份有限公司 通过双功能分子诱导靶蛋白降解的方法
CN107428734A (zh) 2015-01-20 2017-12-01 阿尔维纳斯股份有限公司 用于雄激素受体的靶向降解的化合物和方法
US20170327469A1 (en) 2015-01-20 2017-11-16 Arvinas, Inc. Compounds and methods for the targeted degradation of androgen receptor
US20180140694A1 (en) 2015-05-04 2018-05-24 Bionor Immuno As Dosage regimen for hiv vaccine
WO2016197114A1 (en) 2015-06-05 2016-12-08 Arvinas, Inc. Tank-binding kinase-1 protacs and associated methods of use
HUE065109T2 (hu) 2015-06-26 2024-05-28 Celgene Corp Eljárások Kaposi-szarkóma vagy KSHV-indukált limfóma kezelésére immunomodulátor vegyületek alkalmazásával, valamint biomarkerek alkalmazása
US9809603B1 (en) 2015-08-18 2017-11-07 Deuterx, Llc Deuterium-enriched isoindolinonyl-piperidinonyl conjugates and oxoquinazolin-3(4H)-yl-piperidinonyl conjugates and methods of treating medical disorders using same
US10772962B2 (en) 2015-08-19 2020-09-15 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of bromodomain-containing proteins
NZ742001A (en) * 2015-09-29 2019-06-28 Kangpu Biopharmaceuticals Ltd Pharmaceutical composition and application thereof comprising a benzoheterocyclic compound
WO2017117118A1 (en) 2015-12-28 2017-07-06 Celgene Corporation Compositions and methods for inducing conformational changes in cereblon and other e3 ubiquitin ligases
US10759808B2 (en) 2016-04-06 2020-09-01 The Regents Of The University Of Michigan Monofunctional intermediates for ligand-dependent target protein degradation
CN109415336B (zh) * 2016-04-06 2023-08-29 密执安大学评议会 Mdm2蛋白质降解剂
JP7072519B2 (ja) * 2016-04-12 2022-05-20 ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン Betタンパク質分解剤
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
WO2017197055A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
EP3455219A4 (en) 2016-05-10 2019-12-18 C4 Therapeutics, Inc. AMINE-LINKED C3-GLUTARIMIDE DEGRONIMERS FOR THE DEGRADATION OF TARGET PROTEINS
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
KR102173463B1 (ko) 2016-10-11 2020-11-04 아비나스 오퍼레이션스, 인코포레이티드 안드로겐 수용체의 표적 분해용 화합물 및 방법
CA3042260C (en) 2016-11-01 2023-10-03 Arvinas, Inc. Tau-protein targeting protacs and associated methods of use
BR112019011200B1 (pt) 2016-12-01 2021-12-28 Arvinas Operations, Inc Derivados de tetrahidronaftaleno e tetrahidroisoquinolina como degradadores do receptor de estrogênio
CN110248678A (zh) 2016-12-03 2019-09-17 朱诺治疗学股份有限公司 调节car-t细胞的方法
KR20190104528A (ko) 2016-12-03 2019-09-10 주노 쎄러퓨티크스 인코퍼레이티드 Car-t 세포들 투여를 결정하는 방법
KR20220028178A (ko) 2016-12-16 2022-03-08 강푸 바이오파마슈티칼즈 리미티드 조성물, 이의 적용 및 치료 방법
EP3559002A4 (en) 2016-12-23 2021-02-17 Arvinas Operations, Inc. CHEMERICAL MOLECULES TARGETING EGFR PROTEOLYSIS AND RELATED METHODS OF USE
US10806737B2 (en) 2016-12-23 2020-10-20 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of fetal liver kinase polypeptides
JP2020504741A (ja) 2016-12-23 2020-02-13 アルビナス・オペレーションズ・インコーポレイテッドArvinas Operations, Inc. Raf(急速進行性線維肉腫)ポリペプチドの標的分解のための化合物および方法
US11191741B2 (en) 2016-12-24 2021-12-07 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide
WO2018140809A1 (en) 2017-01-26 2018-08-02 Arvinas, Inc. Modulators of estrogen receptor proteolysis and associated methods of use
KR102125661B1 (ko) * 2017-02-13 2020-06-22 강푸 바이오파마슈티칼즈 리미티드 전립선암 치료용 조합, 약학 조성물 및 치료 방법
PT3618842T (pt) 2017-05-01 2024-01-12 Juno Therapeutics Inc Combinação de uma terapia celular e de um composto imunomodulador
US10093647B1 (en) 2017-05-26 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione dihydrate, compositions and methods of use thereof
EP3630132A1 (en) 2017-06-02 2020-04-08 Juno Therapeutics, Inc. Articles of manufacture and methods for treatment using adoptive cell therapy
CN110769822A (zh) 2017-06-20 2020-02-07 C4医药公司 用于蛋白降解的n/o-连接的降解决定子和降解决定子体
WO2019006427A1 (en) 2017-06-29 2019-01-03 Juno Therapeutics, Inc. WALL MODEL FOR ASSESSING TOXICITIES ASSOCIATED WITH IMMUNOTHERAPIES
CN109422751B (zh) * 2017-09-03 2022-04-22 上海美志医药科技有限公司 一类具有降解酪氨酸蛋白激酶jak3活性的化合物
CN111278815B (zh) 2017-09-04 2024-03-08 C4医药公司 戊二酰亚胺
CN111315735B (zh) 2017-09-04 2024-03-08 C4医药公司 二氢苯并咪唑酮
CN111278816B (zh) 2017-09-04 2024-03-15 C4医药公司 二氢喹啉酮
US10093648B1 (en) 2017-09-22 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione hemihydrate, compositions and methods of use thereof
US10093649B1 (en) 2017-09-22 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione monohydrate, compositions and methods of use thereof
US20200246393A1 (en) 2017-09-28 2020-08-06 Celularity, Inc. Tumor suppression using human placenta-derived intermediate natural killer (pink) cells in combination with an antibody
US12031975B2 (en) 2017-11-01 2024-07-09 Juno Therapeutics, Inc. Methods of assessing or monitoring a response to a cell therapy
WO2019089969A2 (en) 2017-11-01 2019-05-09 Juno Therapeutics, Inc. Antibodies and chimeric antigen receptors specific for b-cell maturation antigen
EP3710002A4 (en) 2017-11-16 2021-07-07 C4 Therapeutics, Inc. DEGRADER AND DEGRONE FOR TARGETED PROTEIN DEGRADATION
US11065231B2 (en) 2017-11-17 2021-07-20 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of interleukin-1 receptor- associated kinase 4 polypeptides
CN111989106A (zh) 2017-12-01 2020-11-24 朱诺治疗学股份有限公司 基因工程化细胞的给药和调节方法
EP3724225A1 (en) 2017-12-15 2020-10-21 Juno Therapeutics, Inc. Anti-cct5 binding molecules and methods of use thereof
KR20200112907A (ko) * 2018-01-25 2020-10-05 가부시키가이샤 후지모토 코포레이션 티오펜 유도체 및 그의 용도
WO2019148055A1 (en) 2018-01-26 2019-08-01 Yale University Imide-based modulators of proteolysis and methods of use
EP3755718A1 (en) 2018-02-21 2020-12-30 Celgene Corporation Bcma-binding antibodies and uses thereof
WO2019191112A1 (en) 2018-03-26 2019-10-03 C4 Therapeutics, Inc. Cereblon binders for the degradation of ikaros
AU2019249231B2 (en) 2018-04-04 2022-04-21 Arvinas Operations, Inc. Modulators of proteolysis and associated methods of use
WO2019204354A1 (en) 2018-04-16 2019-10-24 C4 Therapeutics, Inc. Spirocyclic compounds
WO2019209692A1 (en) * 2018-04-23 2019-10-31 Celgene Corporation Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma
EP3578561A1 (en) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
US11530219B2 (en) 2018-06-29 2022-12-20 Dana-Farber Cancer Institute, Inc. Ligands to cereblon (CRBN)
WO2020051235A1 (en) * 2018-09-04 2020-03-12 C4 Therapeutics, Inc. Compounds for the degradation of brd9 or mth1
AU2019377854A1 (en) 2018-11-08 2021-05-27 Juno Therapeutics, Inc. Methods and combinations for treatment and T cell modulation
AU2019381688A1 (en) * 2018-11-13 2021-06-03 Biotheryx, Inc. Substituted isoindolinones
WO2020102770A1 (en) 2018-11-16 2020-05-22 Juno Therapeutics, Inc. Methods of dosing engineered t cells for the treatment of b cell malignancies
SG11202105502RA (en) 2018-11-30 2021-06-29 Juno Therapeutics Inc Methods for treatment using adoptive cell therapy
CN109293631B (zh) * 2018-11-30 2020-05-08 常州制药厂有限公司 3-氨基-n-(2,6-二氧代-3-哌啶基)-邻苯二甲酰亚胺化合物的制备方法
JP2022518925A (ja) 2019-01-29 2022-03-17 ジュノー セラピューティクス インコーポレイテッド 受容体チロシンキナーゼ様オーファン受容体1(ror1)に特異的な抗体およびキメラ抗原受容体
US20230248696A1 (en) * 2019-05-03 2023-08-10 Dynamic Biologics Inc. Lenalidomide prodrugs, polymeric conjugates, and formulations thereof, and their uses for the treatment of multiple myeloma
WO2020242960A1 (en) 2019-05-24 2020-12-03 Biotheryx, Inc. Compounds targeting proteins and pharmaceutical compositions thereof, and their therapeutic applications
AR119057A1 (es) 2019-05-31 2021-11-17 Celgene Corp Compuestos de 1-oxo-isoindolin-5-carboxamida sustituida, composiciones de estos y métodos de tratamiento con dichos compuestos
JP2022551185A (ja) * 2019-10-09 2022-12-07 モンテ ローザ セラピューティクス アーゲー イソインドリノン化合物
BR112022009514A2 (pt) 2019-11-19 2022-08-16 Bristol Myers Squibb Co Compostos úteis como inibidores de proteína helios
CN118638043A (zh) 2019-12-19 2024-09-13 阿尔维纳斯运营股份有限公司 用于雄激素受体的靶向降解的化合物和方法
EP4146642A1 (en) 2020-05-09 2023-03-15 Arvinas Operations, Inc. Methods of manufacturing a bifunctional compound, ultrapure forms of the bifunctional compound, and dosage forms comprising the same
WO2022152821A1 (en) 2021-01-13 2022-07-21 Monte Rosa Therapeutics Ag Isoindolinone compounds
CN112876414B (zh) * 2021-01-29 2022-09-09 河南大学 一种基于多胺修饰的萘酰亚胺缀合物、其制备方法及应用
WO2022200857A1 (en) * 2021-03-22 2022-09-29 Monte Rosa Therapeutics Ag Pharmaceutical compositions for use in the prevention and treatment of a disease or disorder caused by or associated with one or more premature termination codons
TW202304881A (zh) 2021-04-06 2023-02-01 美商必治妥美雅史谷比公司 經吡啶基取代之側氧基異吲哚啉化合物
WO2022236339A1 (en) * 2021-05-07 2022-11-10 Kymera Therapeutics, Inc. Deuterated irak degraders and uses thereof
CN115504963A (zh) * 2021-06-22 2022-12-23 苏州开拓药业股份有限公司 一种c-Myc蛋白降解剂
WO2023081224A1 (en) * 2021-11-03 2023-05-11 St. Jude Children's Research Hospital, Inc. Substituted n-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-4- yl)methyl)benzamide analogs as modulators of cereblon protein
WO2023147594A2 (en) 2022-01-31 2023-08-03 Kymera Therapeutics, Inc. Irak degraders and uses thereof
CN114656374A (zh) * 2022-02-22 2022-06-24 营口兴福化工有限公司 2,4-二氯-3-氰基-5-氟苯甲酸合成方法
WO2023250400A1 (en) 2022-06-22 2023-12-28 Juno Therapeutics, Inc. Treatment methods for second line therapy of cd19-targeted car t cells
KR20240001071A (ko) * 2022-06-24 2024-01-03 주식회사 아이비스바이오 신규한 탈리도마이드 유도체 및 이의 제조방법
US11957759B1 (en) 2022-09-07 2024-04-16 Arvinas Operations, Inc. Rapidly accelerated fibrosarcoma (RAF) degrading compounds and associated methods of use
WO2024097905A1 (en) 2022-11-02 2024-05-10 Celgene Corporation Methods of treatment with t cell therapy and immunomodulatory agent maintenance therapy
KR20240066904A (ko) * 2022-11-08 2024-05-16 주식회사 온코드바이오 아릴시클로알킬아마이드 구조를 갖는 이소인돌리논 유도체 및 이의 용도

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992014455A1 (en) 1991-02-14 1992-09-03 The Rockefeller University METHOD FOR CONTROLLING ABNORMAL CONCENTRATION TNF α IN HUMAN TISSUES
US5798368A (en) 1996-08-22 1998-08-25 Celgene Corporation Tetrasubstituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines and method of reducing TNFα levels
US5635517B1 (en) 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
CZ304569B6 (cs) * 1996-07-24 2014-07-09 Celgene Corporation 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-aminoisoindolin pro použití pro snížení nežádoucí hladiny TNFα u savce
HU228769B1 (en) * 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
US5874448A (en) * 1997-11-18 1999-02-23 Celgene Corporation Substituted 2-(2,6 dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing TNFα levels
US5955476A (en) * 1997-11-18 1999-09-21 Celgene Corporation Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels
US20030045552A1 (en) * 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof

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