Please help call and write to these companies!

DSAP patients could benefit from new psoriasis drugs or any drug that aims to "normalize" skin. The trouble is that probably nobody cares or is making any effort to get DSAP patients involved with psoriasis drug studies. It's up to us to try to take action. Why wait? Call these companies to see if you can be their guinea pig! Let me know if any let you participate! Click to email me

I subscribe to a newsletter published by the National Psoriasis Foundation. In the September/ October 2000 issue I found this detailed list of new drug treatments being researched.

NPF says that the most promising psoriasis drugs are Amevive and hu1124 which I have highlighted in blue below.

Drug Name Company Description Status
5G1.1 Alexion Pharmaceuticals anti-inflammatory complement inhibitor drug candidate phase 1b
9906 Stiefel topical cream phase 2
ABX-IL8 Abgenix anti-IL8 antibody phase 2
Amevive (alefacept) Biogen fussion protein that binds to CD2 receptor on T cells phase 3
Anti-IGF antisense oligo-nucleotide Centre for Hormone Research (Australia) blocks IGF, epidermal growth regulator preclinical
BCI 202 Bone Care International vitamin D analogue preclinical
BCX34 Biocryst blocks enzyme (PNP) needed for T-cell division (topical) phase 2
Clenoliximab SmithCline Beecham anti CD4 MaB phase 1
Combretastatin A4 Prodrug (CA4P) OXiGENE, Inc. anti-angiogenesis drug phase 1
EGFR & VEGFR inhibitors OSI-Pfiser small molecule inhibitors preclinical
Enbrel (etanercept) Immunex/Wyeth-Ayerst anti-TNF(tumor necrosis factor) drug phase 3
hu1124 (anti-CD11a) Genentech / XOMA 1(888)662-6728 humanized monoclonal antibody against T-cell receptor. phase 3
ICM3 ICOS monoclonal antibody that blocks ICAM-3 phase 1/2
IDEC-114 IDEC Pharmaceuticals monoclonal antibody designed to bind with B7 receptor on antigen presenting cells phase 1/2
IPL4323 Inflazyme oral antinflammatory preclinical
IR502 Immune Response causes the immune system to shut down activated T-cells phase 2
ISIS 2302 ISIS inhibits ICAM-I (topical) phase 2a
LTD-Z-92 Psoraya Pharmaceuticals plant-based topical epidermal keratinocyte antiproliferative phase 1/2
MEDI-507 Medimmune anti-CD2 humanized monoclonal intibody. Study coordinator is Mark Guirrieri (602)437-0097 phase 1 complete
Mycophenolate mofetil (CellCept) Hoffmann-La Roche systemic immunosuppressant investigator initiated trails only
Neovastat (AE-941) Aeterna angiogenesis inhibitor phase 1/2 completed
Olux Connetics steroid (clobetasol propionate) foam FDA approved May 2000
Ontak (DAB3891L2) Ligand Pharmaceuticals IL-2 fusion toxin phase 1/2
Oral Tazarotene Allergan Vitamin A derivative phase 2
Paclitaxel Angiotech Pharmaceuticals anti-cancer drug (topical) phase 1/2
Panretin (alitretinoin) Ligand Pharmaceuticals oral vitamin A derivative phase 2
Panretin (alitretinoin) Ligand Pharmaceuticals topical gel, vitamin A derivative phase 4
Peptide T Advanced Immuni T immunomodulator phase 1/2
PH-10 Photogen Technologies, Inc light sensitizer used with green lights phase 1
Psorgon Nascent Pharmaceuticals (2,5 methyldiethylcinnamate) preclinical
PVAC Corixa  injectable immunomodulatory agent. California 415-476-4701 phase 2
Remicade (infliximab) Centocor anti-TNF (tumor necrosis factor) drug approved for Crohn's disease and Rheumatoid arthritis
SB 33 2235 SmithKline Beecham oral IL-8 antagonist preclinical
Simulect Novartis blocks IL-2 receptors; transplant drug phase 1
SMART Anti-CD3 Protein Design Labs humanized antibody phase 1/2
ST630 Penederm topical vitamin D derivative phase 1 completed
Targretin (bexarotene) Ligand Pharmaceuticals oral vitamin A derivative phase 2
Tenovil (rhulL10) Schering increases levels of IL-10 phase 2
VAS972 Vasogen immunomodulator treats blood removed from body in a medical device and returns it to the body. phase 1/2
VX148 Veertex inhibits IMPDH, which may block T cell proliferation preclinical
Zenapax Protein Design Labs SMART anti-TAC humanized antibody phase 2

 

Phases of drug developement
Preclinical: Extensive laboratory and animal testing by companies to determine biological activity and safety.
Investigational New Drug (IND) application: Describes results of preclinical testing; filed by companies with the FDA prior to initiating testing in people. The IND becomes effective if the FDA does not reject it within 30 days.
Phase 1 clinical trials: Dosing study to establish safe dosage range and to determine how the drug is processed by the body.
Phase 2: Controlled testing to assess effectiveness and safety.
Phase 3: Extensive testing in clinics and hospitals to confirm effectiveness and side effects from use.
New Drug Application (NDA): Files with the FDA after completion of human clinical trials. An NDA usually contains hundreds of thousands of pages of scientific information and clinical data. 

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