- Alovudine
- ALVAC 1433
- AMD070
- AV-1101
- AVX754
- Azodicarbonamide (ADA)
- BMS-488043
- Brecanavir
- Buspirone hydrochloride (Buspar)
- Calanolide A
- Calcium spirulan
- CD4-based therapies
- Cell Genesys gene therapy
- Cimetidine (Dyspamet / Tagamet)
- Colony stimulating factors
- Curcumin
- Dapivirine
- Dextran sulphate
- Dinitrochlorobenzene (DNCB)
- Elvucitabine
- Etravirine
- Extracorporeal photopheresis
- FP-21399
- GPG-NH2
- GS 9137
- GW695634
- GW8248
- HEPT derivatives
- HGP-30
- HGTV43
- Hydroxycarbamide (Hydrea)
- Hyperthermia
- Interferon gamma-1b (Immukin)
- Interleukin-12
- Interleukin-16
- Intravenous immunoglobulin
- Iscador
- Isoprinosine
- JE-2147
- Lentinan
- Malariotherapy
- Maraviroc
- MIV 150
- MK-0518
- MVA-BN-Nef vaccine
- Mycophenolate mofetil (CellCept)
- Ozone
- P-1946
- p24.VLP
- PA-457
- Passive immunotherapy
- Phosphazid
- PN355
- PRO 2000
- PRO 542
- pTHr.HIVA
- Racivir
- Remune
- S-1360
- SJ-3366
- SP1093V
- SPV-30
- Stampidine
- T-1249
- Tat toxoid vaccine
- Thymic peptides
- TMC278
- TNFR:Fc
- TNX-355
- Todoxin
- TSAO derivatives
- Tucaresol
- Vesnarinone
- Vicriviroc
- VIR201
- Virodene P058
- WF10
P-1946
P-1946 is an experimental protease inhibitor, which has shown encouraging results in laboratory studies. It is being developed by a Canadian company called Pharmacor Inc.
In vitro data indicates that P-1946 is fully active against HIV containing primary resistance mutations to amprenavir (Agenerase) and nelfinavir (Viracept). Furthermore, virus which is resistant to other protease inhibitors shows only mild resistance to P-1946. These data suggests that P-1946 may be a useful agent in people with resistance to the existing range of protease inhibitors. No studies in animals or human have yet been reported, so no safety data are available.
References
Sevigny G et al. Activity of a novel anti-HIV protease inhibitor against viral strains resistant to commercially-available drugs. Second International AIDS Society Conference on HIV Pathogenesis and Treatment, Paris, abstract 526, 2003.
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