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UPDATE ON THE MANUFACTURE OF NEW HIV DRUG FUZEON
18-Dec-02
ROCHE RECEIVES FDA CLEARANCE FOR THE COBAS AMPLISCREEN SYSTEM
05-Dec-02
ROCHE RESPONSE TO MSF LETTER
18-Nov-02
NEW DATA INDICATE TREATMENT OF HIV WITH FUZEON SHOULD BE INITIATED BEFORE ALL OTHER TREATMENT OPTIONS DEPLETED
18-Nov-02
FUZEON (ENFUVIRTIDE, T-20) DEMONSTRATES CONSISTENT BENEFIT ACROSS RANGE OF TREATMENT EXPERIENCED HIV PATIENTS
30-Sep-02
REGULATORY FILING IN EUROPEAN UNION FOR FIRST HIV FUSION INHIBITOR FUZEON (T-20)
20-Sep-02
EUROPEAN COMMISSION APPROVES NEW BOOSTED SAQUINAVIR REGIMEN (1000 MG SAQUINAVIR / 100 MG RITONAVIR TWICE DAILY)
19-Sep-02
REGULATORY FILING FOR FIRST HIV FUSION INHIBITOR FUZEON (T-20)
17-Sep-02
ROCHE AND TRIMERIS ANNOUNCE NEXT STEPS IN BRINGING FUZEON (T-20) TO HIV PATIENTS IN NEED OF NEW TREATMENT OPTIONS
02-Aug-02
U.S. FOOD AND DRUG ADMINISTRATION APPROVES NEXT GENERATION HIV-1 TEST
01-Aug-02
FIRST HEAD-TO-HEAD STUDY OF TWO BOOSTED PROTEASE INHIBITORS SHOWS SIGNIFICANT BENEFIT FOR BOOSTED SAQUINAVIR REGIMEN
10-Jul-02
NEW BOOSTED SAQUINAVIR DOSING (1000 MG SAQUINAVIR PLUS 100 MG RITONAVIR BID ) MAINTAINS HIV SUPPRESSION WHILE REDUCING TRIGLYCERIDES AND CHOLESTEROL
10-Jul-02
MAJORITY OF HIV PATIENTS FIND NEW INJECTABLE FUSION INHIBITOR T-20 (ENFUVIRTIDE) EASY TO USE
09-Jul-02
RESEARCHERS IDENTIFY PREDICTIVE AND CLINICAL VALUE OF PROVIRAL HIV-1 DNA QUANTIFICATION FOR HIV PATIENTS
09-Jul-02
NEW T-20 (ENFUVIRTIDE) RESEARCH SIGNALS NEW HOPE FOR CHILDREN AND ADOLESCENTS LIVING WITH HIV
09-Jul-02
FOUR STUDIES EXAMINE STRATEGY OF COMBINING SAQUINAVIR WITH KALETRA� IN TREATMENT-EXPERIENCED HIV PATIENTS
09-Jul-02
TREATMENT EXPERIENCED PATIENTS TWICE AS LIKELY TO ACHIEVE UNDETECTABLE HIV LEVELS WITH T-20 (ENFUVIRTIDE) THAN WITHOUT
08-Jul-02
ROCHE RENEWS ITS COMMITMENT TO THE MULTICENTER AIDS COHORT STUDY
08-Jul-02
ROCHE DIAGNOSTICS SPONSORS SURVEILLANCE PROGRAM TO HELP ENSURE FUTURE PERFORMANCE OF INDUSTRY�S HIV VIRAL LOAD ASSAYS
02-Jul-02
NEW BOOSTED SAQUINAVIR REGIMEN (1000 MG SAQUINAVIR / 100 MG RITONAVIR BID) TO TREAT HIV RECEIVES CPMP POSITIVE OPINION IN THE EU
19-Jun-02
POSITIVE RESULTS FROM SECOND PHASE III STUDY OF HIV FUSION INHIBITOR T-20 (ENFUVIRTIDE)
16-May-02
ROCHE AND TRIMERIS ANNOUNCE 24-WEEK RESULTS FROM FIRST PHASE III STUDY OF HIV FUSION INHIBITOR T-20
18-Apr-02
NEW PROMISING DRUG ADDED TO ROCHE�S STRONG HIV PORTFOLIO
15-Apr-02
STUDY PUBLISHED IN TODAY'S New England Journal of Medicine CONFIRMS ORAL VALCYTE� TREATS AIDS-RELATED EYE DISEASE AS WELL AS IV GANCICLOVIR THERAPY
11-Apr-02
VALCYTE� RECEIVES EU POSITIVE OPINION FOR TREATMENT OF AIDS-RELATED CMV RETINITIS
13-Mar-02
NEW EVIDENCE THAT T-20 ADDS POTENCY TO CONVENTIONAL HIV THERAPIES
19-Feb-02
START OF PILOT PROGRAMME MAY LEAD TO A NEW ERA IN HEALTHCARE DELIVERY FOR AFRICA'S DEVELOPING COUNTRIES
14-Jan-02
A DOUBLE FIRST FOR ROCHE AND TRIMERIS� NEW GROUND-BREAKING HIV FUSION INHIBITORS
19-Dec-01
SWATCH STUDY HIGHLIGHTS IMPORTANCE OF STRATEGIC PLANNING TO OUTWIT HIV RESISTANCE
18-Dec-01
NEW DOSAGE FOR FORTOVASE�/R SHOWS EFFICACY AND EXCELLENT SAFETY PROFILE IN HIV PATIENTS: NEW TREATMENT STRATEGY MAY REDUCE COST OF HIV THERAPY
31-Oct-01
NEW HIV DRUGS - FUSION INHIBITORS - LIKELY TO SUCCESSFULLY TACKLE RESISTANT HIV
30-Oct-01
VALCYTE RECEIVES FIRST EUROPEAN REGULATORY APPROVAL FOR TREATMENT OF AIDS-RELATED CMV RETINITIS
27-Sep-01
PREMIERE HOMOLOGATION EUROPEENNE DE VALCYTE DANS LE TRAITEMENT DE LA RETINITE A CMV LIEE AU SIDA
27-Sep-01
VALCYTE ERSTMALS IN EUROPA F�R DIE BEHANDLUNG DER AIDS-BEDINGTEN CMV-RETINITIS ZUGELASSEN
27-Sep-01
VALCYTE APROBADO POR PRIMERA VEZ EN EUROPA, PARA EL TRATAMIENTO DE LA RETINITIS CITOMEGALOV�RICA RELACIONADA CON EL SIDA
27-Sep-01
ROCHE AND BRAZILIAN MINISTRY OF HEALTH REACH AGREEMENT FOR THE SUPPLY OF HIV DRUG VIRACEPT�
03-Sep-01
ROCHE AND TRIMERIS COMPLETE HIV PHASE III TRIAL RECRUITMENT
09-Aug-01
HIV PATIENTS GIVE GREEN LIGHT TO LONG-TERM USE OF INJECTABLE T-20
11-Jul-01
LARGE VIRACEPT� (NELFINAVIR) STUDY DEMONSTRATES POTENT SUPPRESSION OF HIV AND HIGH PATIENT ADHERENCE OUT TO THREE YEARS OF THERAPY
09-Jul-01
ROCHE AND TRIMERIS BROADEN SCOPE OF HIV PARTNERSHIP
19-Jun-01
NEW DATA REINFORCES BENEFIT OF VIRACEPT IN FIRST LINE THERAPY FOR HIV INFECTION
08-Jun-01
TOP HIV SCIENTISTS MEET TO DISCUSS BETTER LONG TERM TREATMENT OUTCOMES FOR PEOPLE WITH HIV
29-May-01
FOUR STUDIES INVESTIGATE EFFECTIVENESS AND TOLERABILITY OF FORTOVASE�/R AS ONCE- DAILY PROTEASE INHIBITOR FOR HIV INFECTION
09-Apr-01
NEW INITIATIVE CREATES ACCESS TO HIV CARE AND TREATMENT IN FOUR AFRICAN COUNTRIES
28-Feb-01
NEW DATA CONFIRMS HIGHLY EFFECTIVE AND TOLERABLE ROLE OF VIRACEPT� IN FIRST LINE TREATMENT STRATEGIES OF HIV INFECTION
08-Feb-01
ROCHE HIV PROTEASE INHIBITOR SAQUINAVIR SHOWS GREATER IN VITRO POTENCY THAN NEW DRUG LOPINAVIR
23-Oct-00
CALL TO ACTION: ROCHE ADVOCATES DEVELOPMENT OF HIV DRUG POTENCY GUIDELINES TO HELP PHYSICIANS MAKE OPTIMAL TREATMENT DECISIONS
23-Oct-00
IMPORTANT PROGRESS IN TREATMENT OF HIV INFECTION TO BE REPORTED
10-Jul-00
BLOOD LEVELS OF FORTOVASE INCREASE WITH A MINI-DOSE OF RITONAVIR
15-Jun-00
INVESTIGATIONAL AIDS-RELATED ORAL DRUG VALGANCICLOVIR PROVIDES COMPARABLE RESULTS TO INTRAVENOUS CYMEVENE
03-Feb-00
SHIFTING TREATMENT DEMOGRAPHICS HIGHLIGHT NEED TO MANAGE LONG-TERM HIV TREATMENT OPTIONS
02-Feb-00
VIRACEPT COMBINATION IN PREGNANT WOMEN PREVENTS HIV INFECTION IN NEWBORNS, EARLY STUDY SHOWS
02-Feb-00
ROCHE AND TRIMERIS REPORT CLINICAL PROGRESS IN DEVELOPMENT OF HIV FUSION INHIBITORS
01-Feb-00
NEW STUDIES SHOW REAL-LIFE ADVANTAGES OF VIRACEPT IN EFFICACY, TOLERABILITY, DRUG RESISTANCE AND CONVENIENCE
26-Oct-99
VIRACEPT TWICE-DAILY DOSING SHOWS LONG-TERM ANTI-HIV EFFECTIVENESS, STUDY SHOWS
26-Oct-99
NEW FUSION INHIBITOR T-20 COMBINATION REGIMEN REDUCES HIV LEVELS IN HEAVILY PRE-TREATED PATIENTS
25-Oct-99
FORTOVASE ONCE-A-DAY DOSING SHOWS PROMISE IN FIRST STUDY IN HIV-POSITIVE INDIVIDUALS
25-Oct-99
TREATMENT INCLUDING FORTOVASE SHOWS SIGNIFICANT PROMISE TO ELIMINATE HIV TRANSMISSION FROM MOTHER TO INFANT
25-Oct-99
STUDY HIGHLIGHTS POTENTIAL FOR MORE CONVENIENT ONCE-A-DAY ADMINISTRATION
25-Oct-99
BACKGROUND INFORMATION: T-20 FACT SHEET
27-Sep-99
SIXTEEN-WEEK ANALYSIS OF HEAVILY PRE-TREATED PATIENTS RECEIVING T-20 AS A COMPONENT OF MULTI-DRUG SALVAGE THERAPY (T20-205)
27-Sep-99
BACKGROUND INFORMATION: CROSS RESISTANCE DATA PRESENTED AT ICAAC SUPPORT FIRST-LINE USE OF VIRACEPT
27-Sep-99
DATA PRESENTED AT ICAAC SUPPORT FIRST-LINE USE OF VIRACEPT
27-Sep-99
NEW AIDS STUDY SUGGESTS T-20-CONTAINING REGIMENS REDUCES HIV IN HEAVILY PRE-TREATED PATIENTS
27-Sep-99
BACKGROUND INFORMATION: FORTOVASE (Saquinavir) STUDY HIGHLIGHTS POTENTIAL FOR MORE CONVENIENT ONCE-A-DAY ADMINISTRATION
26-Sep-99
STRONG PROMISE FOR ONCE-A-DAY DOSING OF FORTOVASE, STUDY SHOWS
26-Sep-99
ROCHE AND TRIMERIS SIGN AGREEMENT TO DEVELOP TRIMERIS'S COMPOUNDS
12-Jul-99
FUSION INIHIBITORS: BACKGROUND INFORMATION
12-Jul-99
FUSION INHIBITORS:T-20 AND T-1249 BACKGROUND INFORMATION
12-Jul-99
MAJOR ADVANCE IN HIV MANAGEMENT: PAN EUROPEAN HIV GENOTYPING THRUST LAUNCHED
08-May-99
BACKGROUND INFORMATION: FORTOVASE� (SAQUINAVIR): CLINICAL STUDIES HIGHLIGHT NEW FORMULATION'S POWER AND CONVENIENCE
08-May-99
BACKGROUND INFORMATION: GENOTYPING
08-May-99
BACKGROUND INFORMATION: ROCHE VIROLOGY NETWORK AND PE BIOSYSTEMS ANNOUNCE THE GREAT TRIAL
08-May-99
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