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1
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0030869269
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Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy
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Gulick RM, Mellors JW, Havlir D et al. Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy. N Engl J Med 1997;337: 734-739.
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(1997)
N Engl J Med
, vol.337
, pp. 734-739
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Gulick, R.M.1
Mellors, J.W.2
Havlir, D.3
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2
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6544242025
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Dramatically declining morbidity and mortality in an ambulatory HIV-infected population
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Abstract 12343, Geneva, June
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Pallela F, Moorman A, Delaney R et al. Dramatically declining morbidity and mortality in an ambulatory HIV-infected population. (Abstract 12343) 12th World Conference, Geneva, June 1998.
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(1998)
12th World Conference
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Pallela, F.1
Moorman, A.2
Delaney, R.3
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3
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0032189850
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Adverse effects of reverse transcriptase inhibitors: Mitochondrial toxicity as common pathway
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Brinkman K, ter Hoftede HJM, Burger DM et al. Adverse effects of reverse transcriptase inhibitors: mitochondrial toxicity as common pathway. AIDS 1998; 12: 1735-1744.
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(1998)
AIDS
, vol.12
, pp. 1735-1744
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Brinkman, K.1
Ter Hoftede, H.J.M.2
Burger, D.M.3
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5
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6544235831
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Safety and pharmacokinetics of nevirapine in neonates born to HIV-1 infected women
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Abstract 533, Washington, January
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Mirochnik M and the ACTG Protocol 250 Team. Safety and pharmacokinetics of nevirapine in neonates born to HIV-1 infected women. (Abstract 533) 4th Conference on Retrovirusees and Opportunistic Infections, Washington, January 1997.
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(1997)
4th Conference on Retrovirusees and Opportunistic Infections
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Mirochnik, M.1
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6
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8944232862
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Randomized, controlled Phase I/II trial of combination therapy with delavirdine (U-90152S) and conventional nucleosides in human immunodeficiency virus type-1-infected patients
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Davey RT, Chaitt DG, Reed GF et al. Randomized, controlled Phase I/II trial of combination therapy with delavirdine (U-90152S) and conventional nucleosides in human immunodeficiency virus type-1-infected patients. Antimicrob Agents Chemother 1996; 40: 1657-1664.
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(1996)
Antimicrob Agents Chemother
, vol.40
, pp. 1657-1664
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Davey, R.T.1
Chaitt, D.G.2
Reed, G.F.3
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8
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0002845384
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Suppression of viral load in the genital tract and cerebrospinal fluid (CSF) in patients on combination therapy including efavirenz
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Poster 0554, Berlin, March
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Tashima K, Cu-Uvin S, Callendo A et al. Suppression of viral load in the genital tract and cerebrospinal fluid (CSF) in patients on combination therapy including efavirenz. (Poster 0554) 9th European Conference of Clinical Microbiology and Infectious Diseases, Berlin, March 1999.
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(1999)
9th European Conference of Clinical Microbiology and Infectious Diseases
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Tashima, K.1
Cu-Uvin, S.2
Callendo, A.3
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10
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0032565098
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A randomized, double-blind trial comparing combination of nevirapine, didanosine and zidovudine for HIV-infected patients. The INCAS trial
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Montaner JSG, Reiss P, Cooper S et al. A randomized, double-blind trial comparing combination of nevirapine, didanosine and zidovudine for HIV-infected patients. The INCAS trial. J Am Med Assoc 1998; 279: 930-937.
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(1998)
J Am Med Assoc
, vol.279
, pp. 930-937
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Montaner, J.S.G.1
Reiss, P.2
Cooper, S.3
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11
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0001968195
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The Atlantic Study: A randomized open-label study comparing two protease inhibitors (PI)-sparing antiretroviral strategies versus a standard PI-containing regimen
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Abstract 18, Chicago, February
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Katlama C, Murphy R, Johnson V et al. The Atlantic Study: a randomized open-label study comparing two protease inhibitors (PI)-sparing antiretroviral strategies versus a standard PI-containing regimen. (Abstract 18) 6th Conference on Retroviruses and Opportunistic Infections, Chicago, February 1999.
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(1999)
6th Conference on Retroviruses and Opportunistic Infections
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Katlama, C.1
Murphy, R.2
Johnson, V.3
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12
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0003262944
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Durable clinical anti-HIV-1 activity (72 weeks) and tolerability for efavirenz (DMP 266) in combination with (IDV) [DMP 266-003, Cohort IV]
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Poster 12359, Geneva, June
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Riddler S, Kahn J, Hicks C et al. Durable clinical anti-HIV-1 activity (72 weeks) and tolerability for efavirenz (DMP 266) in combination with (IDV) [DMP 266-003, Cohort IV]. (Poster 12359) 12th World AIDS Conference, Geneva, June 1998.
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(1998)
12th World AIDS Conference
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Riddler, S.1
Kahn, J.2
Hicks, C.3
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13
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0003358035
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A Phase II, double-blind, placebo-controlled, dose ranging study to assess the antiretroviral activity and safety of efavirenz (EFV, SUSTIVA™, DMP 266) in combination with open-label zidovudine (ZDV) with lamivudine (3TC) at 36 weeks [DMP 266-005]
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Poster 22334 Geneva, June
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Haas DW, Seekins D, Cooper R et al. A Phase II, double-blind, placebo-controlled, dose ranging study to assess the antiretroviral activity and safety of efavirenz (EFV, SUSTIVA™, DMP 266) in combination with open-label zidovudine (ZDV) with lamivudine (3TC) at 36 weeks [DMP 266-005]. (Poster 22334) 12th World AIDS Conference, Geneva, June 1998.
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(1998)
12th World AIDS Conference
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Haas, D.W.1
Seekins, D.2
Cooper, R.3
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14
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0003322084
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A Phase III, Multicenter, randomized, openlabel study to compare the antiretroviral activity and tolerability of efavirenz (EFV) + indinavir (IDV), versus EFV + zidovudine (ZDV) + lamivudine (3TC), versus IDV + ZDV + 3TC at 24 weeks [DMP 266-006]
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Poster 22336 Geneva, June
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Staszewski S, Morales-Ramirez J, Tashima K et al. A Phase III, Multicenter, randomized, openlabel study to compare the antiretroviral activity and tolerability of efavirenz (EFV) + indinavir (IDV), versus EFV + zidovudine (ZDV) + lamivudine (3TC), versus IDV + ZDV + 3TC at 24 weeks [DMP 266-006]. (Poster 22336) 12th World AIDS Conference Geneva, June 1998.
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(1998)
12th World AIDS Conference
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Staszewski, S.1
Morales-Ramirez, J.2
Tashima, K.3
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15
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4244108957
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A Phase III, double-blind, placebo-controlled, multicenter study to determine the effectiveness and tolerability of the combination of efavirenz (EFV, SUSTIVA ™, DMP 266) and indinavir (IDV) versus indinavir in HIV-1 infected patients receiving nucleoside analogue (NRTI) therapy at 24 weeks [DMP 266-020]
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Poster 22343 Geneva, June
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Fesel WJ, Haas DW, Delapenha RA et al. A Phase III, double-blind, placebo-controlled, multicenter study to determine the effectiveness and tolerability of the combination of efavirenz (EFV, SUSTIVA ™, DMP 266) and indinavir (IDV) versus indinavir in HIV-1 infected patients receiving nucleoside analogue (NRTI) therapy at 24 weeks [DMP 266-020]. (Poster 22343) 12th World AIDS Conference, Geneva, June 1998.
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(1998)
12th World AIDS Conference
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Fesel, W.J.1
Haas, D.W.2
Delapenha, R.A.3
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16
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0003290066
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Ziagen/Combivir is equivalent to indinavir/combivir in antiretroviral therapy naïve adults at 24 weeks (CNA3005)
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Abstract 20, Chicago, February
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Staszewski S, Keiseer P, Gathe E et al. Ziagen/Combivir is equivalent to indinavir/combivir in antiretroviral therapy naïve adults at 24 weeks (CNA3005). (Abstract 20) 6th Conference on Retroviruses and Opportunistic Infections, Chicago, February 1999.
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(1999)
6th Conference on Retroviruses and Opportunistic Infections
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Staszewski, S.1
Keiseer, P.2
Gathe, E.3
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