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HIV Pipeline: Chart on drugs in development

Research Initiative Treatment Action (RITA!); Vol 8, No. 1 Summer 2002
Source: Ben Cheng, Project Inform *



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-3465°

CXCR4 antagonist

Preclinical

AnorMed

AMD-8445°

entry inhibitor

Preclinical

AnorMed

Atazanavir (BMS-232623)

protease inhibitor

Phase 2 – 3*

Bristol-Myers Squibb

BCH-10618 (DOTC)

nucleoside analog RT inhibitor

Preclinical

Shire Biochem

BEA-005°

nucleoside analog RT inhibitor

Preclinical

Medivir

Beta-D-Fd4C°

nucleoside analog RT inhibitor

Preclinical

Vion

Beta-L-Fd4C°

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 Pharmaceuticals**

DPC 681

protease inhibitor

Preclinical

Dupont Pharmaceuticals**

DPC 684

protease inhibitor

Preclinical

Dupont Pharmaceuticals**

DPC 961

non-nucleoside RT inhibitor

Phase 1

DuPont Pharmaceuticals**

Emivirine (MKC-442)

non-nucleoside RT inhibitor

Phase 3

Triangle Pharmaceuticals

Emtricitabine (FTC)

nucleoside analog RT inhibitor

Phase 3

Triangle Pharmaceuticals

HI-236°

non-nucleoside RT inhibitor

Preclinical

Wayne Hughes Institute

Hu5A8°

binding inhibitor

Preclinical

Tanox

Hydroxyurea

inhibits cellular factors

Phase 2 – 3

Bristol-Myers Squibb

L-870,810

integrase inhibitor

Phase 1

Merck & Co.

LB-71350°

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 3*

Trimeris/Roche

Phosphazid°

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

RD4-2217°

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-3366°

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-781°

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



Note
: RT stands for Reverse Transcriptase

* Available in expanded access

** Dupont Pharmaceuticals sold its anti-HIV drug Sustiva and its HIV research pipeline to Bristol-Myers Squibb in 2001

° No information available

* Ben Cheng is now the Project Manager at the Forum for Collaborative HIV Research in Washington, DC (hivforum.org).

20020710
RI020707


Copyright © 2002 - Research Initiative Treatment Action (RITA!). Reproduced with permission. RITA! is published by The Center for AIDS. Contact Thomas Gegeny, MS, ELS, Editor, RITA! for permission to reproduce RITA!. tom@centerforaids.org. http://www.centerforaids.org

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