IL125442A - A method for selecting optimal HIV inhibitors for use in the chemotherapy of HIV-positive patients - Google Patents
A method for selecting optimal HIV inhibitors for use in the chemotherapy of HIV-positive patientsInfo
- Publication number
- IL125442A IL125442A IL12544297A IL12544297A IL125442A IL 125442 A IL125442 A IL 125442A IL 12544297 A IL12544297 A IL 12544297A IL 12544297 A IL12544297 A IL 12544297A IL 125442 A IL125442 A IL 125442A
- Authority
- IL
- Israel
- Prior art keywords
- hiv
- inhibitors
- chimeric
- inhibitor
- patient
- Prior art date
Links
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Classifications
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- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
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- C12N2740/00—Reverse transcribing RNA viruses
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PCT/IB1997/000071 WO1997027480A1 (en) | 1996-01-26 | 1997-01-24 | Method of managing the chemotherapy of patients who are hiv positive based on the phenotypic drug sensitivity of human hiv strains |
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TR (1) | TR199801443T2 (hu) |
WO (1) | WO1997027480A1 (hu) |
ZA (1) | ZA97669B (hu) |
Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100336699B1 (ko) | 1992-08-25 | 2002-05-13 | 윌리암스 로저 에이 | 레트로바이러스 프로테아제 저해제로서 유용한히드록시에틸아미노 술폰아미드 |
US20030220276A1 (en) * | 1995-05-16 | 2003-11-27 | Opendra Narayan | HIV vaccine and method of use |
US6242187B1 (en) | 1996-01-29 | 2001-06-05 | Virologic, Inc. | Compositions and methods for determining anti-viral drug susceptibility and resistance and anti-viral drug screening |
US20070010471A1 (en) * | 1997-05-02 | 2007-01-11 | Opendra Narayan | HIV DNA vaccine |
WO1999006597A1 (en) * | 1997-07-30 | 1999-02-11 | Virologic, Inc. | Compositions and methods for determining anti-viral drug susceptibility and resistance and anti-viral drug screening |
CA2329140A1 (en) * | 1998-05-26 | 1999-12-02 | Virologic, Inc. | Means and methods for monitoring non-nucleoside reverse transcriptase inhibitor antiretroviral therapy |
JP2003501051A (ja) * | 1999-05-28 | 2003-01-14 | ビルコ・エヌ・ブイ | 表現型薬物耐性と相関するhiv−1逆転写酵素における新規な変異プロフィル |
US6800437B1 (en) | 1999-08-06 | 2004-10-05 | Tibotec Bvba | Method of monitoring a biological system by labeling with an apo metal binding protein |
EP1109019A1 (en) * | 1999-12-15 | 2001-06-20 | BioStrands S.r.l. | Method to evaluate the sensitivity of HIV variants to drugs able to inhibit the HIV protease |
WO2001057245A2 (en) * | 2000-02-04 | 2001-08-09 | K.U.Leuven Research & Development | Hiv-1 resistance assay |
GB0009374D0 (en) * | 2000-04-14 | 2000-05-31 | Glaxo Group Ltd | Phenotyping assay and reagents therefor |
US7206699B2 (en) | 2000-04-18 | 2007-04-17 | Virco N.V. | Methods for measuring therapy resistance |
AU2001256318B8 (en) * | 2000-04-20 | 2007-03-22 | Virco Bvba | Method for mutation detection in HIV using pol sequencing |
US6800463B1 (en) * | 2000-04-20 | 2004-10-05 | Virco Bvba | Method for mutation detection in HIV-1 using pol sequencing |
US6582901B2 (en) * | 2000-04-26 | 2003-06-24 | Bruce K. Patterson | Cell specific anti-viral drug susceptibility test using tagged permissive target cells |
US7058616B1 (en) | 2000-06-08 | 2006-06-06 | Virco Bvba | Method and system for predicting resistance of a disease to a therapeutic agent using a neural network |
AU2001266863A1 (en) * | 2000-06-12 | 2001-12-24 | Virologic, Inc. | Means and methods for monitoring antiretroviral therapy and guiding therapeutic decisions in the treatment of hiv/aids |
US6582920B2 (en) * | 2000-09-01 | 2003-06-24 | Gen-Probe Incorporated | Amplification of HIV-1 RT sequences for detection of sequences associated with drug-resistance mutations |
EP1356082A2 (en) | 2000-10-20 | 2003-10-29 | Virco Bvba | Mutational profiles in hiv-1 reverse transcriptase correlated with phenotypic drug resistance |
AU2002212344B2 (en) * | 2000-10-20 | 2007-05-17 | Virco Bvba | Establishment of biological cut-off values for predicting resistance to therapy |
US6958211B2 (en) * | 2001-08-08 | 2005-10-25 | Tibotech Bvba | Methods of assessing HIV integrase inhibitor therapy |
US7306901B2 (en) | 2001-08-08 | 2007-12-11 | Tibotec Pharmaceuticals, Ltd. | Methods and means for assessing HIV envelope inhibitor therapy |
ATE389029T1 (de) | 2001-11-08 | 2008-03-15 | Tibotec Pharm Ltd | Protease assay zur kontrolle medikamentöser therapie |
DE60327768D1 (de) | 2002-07-01 | 2009-07-09 | Tibotec Pharm Ltd | Mutationsprofile bei mit phänotypischer medikamentenresistenz korrelierter hiv-1-protease |
US7473524B2 (en) | 2002-07-01 | 2009-01-06 | Hilde Azijn | Mutational profiles in HIV-1 protease correlated with phenotypic drug resistance |
EP1728186A2 (en) | 2004-03-02 | 2006-12-06 | Virco Bvba | Estimation of clinical cut-offs |
AU2006323930B2 (en) | 2005-12-07 | 2012-06-21 | Janssen Sciences Ireland Uc | Methods, plasmid vectors and primers for assessing HIV viral fitness |
AU2007239535B2 (en) * | 2006-04-14 | 2012-12-20 | Tibotec Pharmaceuticals Ltd. | Methods and means for assessing HIV gag/protease inhibitor therapy |
CA2688278A1 (en) | 2007-05-25 | 2008-12-04 | Tibotec Pharmaceuticals | New mutational profile in hiv-1 gag cleavage site correlated with phenotypic drug resistance |
ES2546190T3 (es) * | 2008-10-06 | 2015-09-21 | Janssen Diagnostics Bvba | Método para determinar mutaciones de resistencia a fármacos en cualquiera de las regiones de proteína no estructural NS3 a NS5B del virus de la hepatitis C (HCV) para los genotipos 1 a 6 |
AU2010247444A1 (en) * | 2009-05-12 | 2011-11-24 | Virco Bvba | HIV-1-C resistance monitoring |
CN107085093B (zh) * | 2017-03-24 | 2019-06-21 | 西藏诺迪康药业股份有限公司 | 重组人白细胞介素1受体拮抗剂滴眼液生物学活性的检测方法 |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3875396A (en) | 1973-11-12 | 1975-04-01 | Illuminite Corp | Illuminated clipboard |
US4675147A (en) * | 1983-04-06 | 1987-06-23 | Westinghouse Electic Corp. | Generating an integrated graphic display of the safety status of a complex process plant |
US5716826A (en) * | 1988-03-21 | 1998-02-10 | Chiron Viagene, Inc. | Recombinant retroviruses |
US5665577A (en) | 1989-02-06 | 1997-09-09 | Dana-Farber Cancer Institute | Vectors containing HIV packaging sequences, packaging defective HIV vectors, and uses thereof |
KR100215949B1 (ko) | 1989-05-25 | 1999-08-16 | 로버트 엘. 타버 | 유전자기능의다가억제제 |
US5401629A (en) | 1990-08-07 | 1995-03-28 | The Salk Institute Biotechnology/Industrial Associates, Inc. | Assay methods and compositions useful for measuring the transduction of an intracellular signal |
JPH05148202A (ja) * | 1991-04-10 | 1993-06-15 | Tsumura & Co | 新規な化合物およびその医薬としての用途 |
AU4248593A (en) | 1992-05-14 | 1993-12-13 | Mark Holodniy | Polymerase chain reaction assays for monitoring antiviral therapy |
US5733720A (en) | 1992-06-18 | 1998-03-31 | Washington University | Genetically engineered cell lines for detecting infectious herpesvirus and methods therefor |
DE69316368T2 (de) | 1992-07-06 | 1998-06-25 | Harvard College | Verfahren und diagnostische kits zur bestimmung der toxizität einer verbindung unter verwendung von an bakterielle stresspromotoren fusionierten reportergenen |
US5344846A (en) | 1992-12-30 | 1994-09-06 | The United States Of America As Represented By The Department Of Health And Human Services | Compositions and methods for inhibiting deoxyhypusine synthase and the growth of cells |
US5591579A (en) | 1993-12-21 | 1997-01-07 | Washington University | Indicator cell line for detecting RNA viruses and method therefor |
US6063562A (en) * | 1994-09-16 | 2000-05-16 | Sepracor, Inc. | In vitro method for predicting the evolutionary response of HIV protease to a drug targeted thereagainst |
US5569588A (en) | 1995-08-09 | 1996-10-29 | The Regents Of The University Of California | Methods for drug screening |
CA2232086A1 (en) | 1995-09-15 | 1997-04-03 | Samir Chachoua | Method for the identification and therapeutic use of disease-associated organisms, elements and forces |
US5885806A (en) * | 1995-11-28 | 1999-03-23 | The Johns Hopkins University School Of Medicine | Methods to prepare conditionally replicating viral vectors |
DE69739645D1 (de) | 1996-01-29 | 2009-12-17 | Monogram Biosciences Inc | Verfahren zur Bestimmung antiviraler Wirkstoff Suszeptibilität und Resistenz sowie antivirales Wirkstoff-Screening |
US5837464A (en) | 1996-01-29 | 1998-11-17 | Virologic, Inc. | Compositions and methods for determining anti-viral drug susceptibility and resistance and anti-viral drug screening |
US5945276A (en) | 1996-04-10 | 1999-08-31 | Signal Pharmaceuticals, Inc. | Reporter cell line system for detecting cytomegalovirus and identifying modulators of viral gene expression |
US5939253A (en) | 1996-04-26 | 1999-08-17 | Diagnostic Hybrids, Inc. | Compositions and methods for detecting viral infection |
JP2001522454A (ja) | 1997-04-07 | 2001-11-13 | バイオイメージ エイ/エス | 細胞応答への影響に関する定量情報の抽出方法 |
WO1998046796A1 (en) | 1997-04-11 | 1998-10-22 | The Regents Of The University Of California | A method of screening nucleotide sequences to identify disruptors or effectors of biological processes or pathways |
WO1998059074A1 (en) | 1997-06-23 | 1998-12-30 | Emory University | Human immunodeficiency viruses causing aids in a nonhuman primate |
US5976813A (en) | 1997-12-12 | 1999-11-02 | Abbott Laboratories | Continuous format high throughput screening |
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- 1997-01-24 SK SK1002-98A patent/SK283878B6/sk not_active IP Right Cessation
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