| Compound |
Class of Compound |
Phase of Development |
Pharmaceutical Company |
| ACH-126,443 (L-Fd4C) |
nucleoside analog RT inhibitor |
Phase 1 |
Achilleon |
| ADA |
zinc finger |
Phase 1-2 |
Hubriphar |
| AMD-34653
|
CXCR4 antagonist |
Preclinical |
AnorMed |
| AMD-84453
|
entry inhibitor |
Preclinical |
AnorMed |
| Atazanavir (BMS-232623) |
protease inhibitor |
Phase 2-31
|
Bristol-Myers Squibb |
| BCH-10618 (DOTC) |
nucleoside analog RT inhibitor |
Preclinical |
Shire Biochem |
| BEA-0053
|
nucleoside analog RT inhibitor |
Preclinical |
Medivir |
| Beta-D-Fd4C3
|
nucleoside analog RT inhibitor |
Preclinical |
Vion |
| Beta-L-Fd4C3
|
nucleoside analog RT inhibitor |
Preclinical |
Vion |
| BMS-806 |
entry inhibitor |
Phase 1 |
Bristol-Myers Squibb |
| Calanolide A |
non-nucleoside RT inhibitor |
Phase 2 |
Sarawak Medichem |
| Capravirine |
non-nucleoside RT inhibitor |
Phase 2 |
Pfizer/Agouron |
| DAPD |
nucleoside analog RT inhibitor |
Phase 1-2 |
Triangle Pharmaceuticals |
| DEHSPM |
inhibits hypusin/eIF-5A |
Phase 1 |
SunPharm |
| DPC 083 |
non-nucleoside RT inhibitor |
Phase 1-2 |
DuPont Pharmaceuticals2
|
| DPC 681 |
protease inhibitor |
Preclinical |
Dupont Pharmaceuticals2
|
| DPC 684 |
protease inhibitor |
Preclinical |
Dupont Pharmaceuticals2
|
| DPC 961 |
non-nucleoside RT inhibitor |
Phase 1 |
DuPont Pharmaceuticals2
|
| Emivirine (MKC-442) |
non-nucleoside RT inhibitor |
Phase 3 |
Triangle Pharmaceuticals |
| Emtricitabine (FTC) |
nucleoside analog RT inhibitor |
Phase 3 |
Triangle Pharmaceuticals |
| HI-2363
|
non-nucleoside RT inhibitor |
Preclinical |
Wayne Hughes Institute |
| Hu5A83
|
binding inhibitor |
Preclinical |
Tanox |
| Hydroxyurea |
inhibits cellular factors |
Phase 2-3 |
Bristol-Myers Squibb |
| L-870,810 |
integrase inhibitor |
Phase 1 |
Merck & Co. |
| LB-713503
|
protease inhibitor |
Preclinical |
LG Chemical |
| Mycophenlate |
inhibits cellular factors |
Phase 1-2 |
Hoffman-La Roche |
| Peldesine |
inhibits cellular factors |
Phase 1 |
Biocryst |
| Pentfuside (T-20) |
fusion inhibitor |
Phase 31
|
Trimeris/Roche |
| Phosphazid3
|
nucleoside analog RT inhibitor |
Preclinical |
Viscount |
| PNU142721 |
non-nucleoside RT inhibitor |
Preclinical |
Pharmacia |
| PRO 140 |
CCR5 antagonist |
Preclinical |
Progenics |
| PRO 367 |
entry inhibitor |
Phase 1 |
Progenics |
| PRO 542 |
attachment inhibitor |
Phase 1-2 |
Progenics |
| RD4-22173
|
non-nucleoside RT inhibitor |
Preclinical |
Tosoh |
| Resveratrol |
inhibits cellular factors |
Phase 1 |
Pharmascience |
| S-1360 |
integrase inhibitor |
Phase 1-2 |
Shionogi Pharmaceuticals |
| SCH C |
CCR5 antagonist |
Phase 1 |
Schering Plough |
| SCH D |
CCR5 antagonist |
Preclinical |
Schering Plough |
| SJ-33663
|
non-nucleoside RT inhibitor |
Preclinical |
Samjin |
| T-1249 |
fusion inhibitor |
Phase 1 |
Trimeris/Roche |
| TAK 449 |
CCR5 antagonist |
Preclinical |
Takeda |
| Tipranavir |
protease inhibitor |
Phase 1-2 |
Boehringer Ingelheim |
| TMC 125 |
non-nucleoside RT inhibitor |
Phase 2 |
Tibotec Virco |
| TMC 120 |
non-nucleoside RT inhibitor |
Phase 2 |
Tibotec Virco |
| TMC 126 |
protease inhibitor |
Phase 1 |
Tibotec Virco |
| UC-7813
|
non-nucleoside RT inhibitor |
Preclinical |
Uniroyal |
| UK-427,857 |
CCR5 antagonist |
Preclinical |
Pfizer |
| VX-175/GW433908 (amprenavir prodrug) |
protease inhibitor |
Phase 2-3 |
Vertex/GlaxoSmithKline |