 
13 
mors. Aranesp increases hemoglobin 
and decreases the need for transfu-
sions. Current standard of care re-
quires that cancer patients receive in-
jections of the currently available ane-
mia therapy three times every week, 
although many patients are receiving 
just weekly injections.  
On December 18, Amgen and 
Immunomedics announced that the 
companies have signed an agreement 
to license to Amgen a novel cancer 
therapeutic antibody for the treatment 
of low-grade and aggressive non-
Hodgkin's lymphoma (NHL), devel-
oped by Immunomedics. The human-
ized antibody, Epratuzumab, is being 
studied in a pivotal clinical trial to 
treat low-grade NHL patients who 
either do not respond, or who do not 
have a durable response, to the cur-
rently available antibody therapy, Ri-
tuxan (IDEC/Genentech). Epratuzu-
mab will also be studied in a pivotal 
trial in patients with aggressive NHL 
who have previously received other 
therapy. Epratuzumab is also in a 
Phase I/II study in combination with 
Rituxan in low-grade and aggressive 
NHL patients who have not previously 
been treated with an antibody-based 
product.  
Early-phase clinical studies sug-
gest that Epratuzumab may provide 
greater ease of administration than 
Rituxan by having a shorter infusion 
time. Epratuzumab binds to a differ-
ent cell-surface protein (CD22) than 
Rituxan (CD20). 
 
December 4, studies were re-
leased on 
Celgene's (BSR #39:  Phase 
III Cancer) Thalomid at the American 
Wall Street is anticipating a slow 
down of the economy and worse yet, a 
recession. Uncertainty abounds. Can 
the pharmaceutical companies, who 
lately have had a nice run, sustain 
their momentum?  And when Celera 
publishes its paper on mapping the 
human genome in 
Science early next 
year -- will that be the catalyst to 
cause a rotation out of Big Pharma 
back into biotechs? 
Lately, so much speculation has 
been factored into the market and 
translating into apprehension that the 
valuation of biotech stocks appears to 
be in limbo. Factors such as the value 
of patent/intellectual property or the 
impact of genomics continue to loom 
and instill questions about biotechs' 
future. Currently the market's vision 
is clouded with short-term outlooks, 
but remember, in the year 2000, many 
biotech companies, were able to line 
their accounts with cash to be used to 
move forward in businesses, and de-
veloping their businesses.  Investors 
of biotechs must remember, current 
therapeutics treat the "symptoms" of 
the disease, not the underlying 
mechanism of the disease itself.  The 
biotech movement goal is toward un-
derstanding the disease, thus improv-
ing upon existing treatments finding 
cures.  
 
               
On December 28, 
Abgenix (BSR 
#35:  Psoriasis) started a Phase IIa 
multi-center clinical trial of ABX-IL8 
iin patients with rheumatoid arthritis. 
The Phase IIa trial is a double-blind, 
placebo-controlled study designed to 
evaluate the efficacy and safety of 
ABX-IL8 in rheumatoid arthritis. The 
company is also conducting a Phase 
IIa clinical trial with ABX-IL8 in pa-
tients with moderate-to-severe psoria-
sis, and expects to report results of 
this study in the first quarter of 2001.  
 
December 4, 
Alexion (BSR #31:  
Transplantation) announced preclini-
cal data at the American Society of 
Hematology showing that its anti-
inflammatory C5 Inhibitor signifi-
cantly prevented loss of platelets, im-
portant blood cells responsible for 
normal clotting, in chronic immune 
thrombocytopenia purpura. The re-
sults suggest that C5 Inhibitor may 
substantially prevent clotting compli-
cations with other autoimmune disor-
ders, as well as lupus, and thrombocy-
topenic purpura. If successfully devel-
oped, these results would further 
broaden Alexion's portfolio of autoim-
mune disorders potentially address-
able with its C5 Inhibitor therapy, 
which currently includes five different 
clinical autoimmune disease pro-
grams. 
Alexion's technology is prom-
ising, but shares are still trading at 
lofty prices.  
 
December 4, 
Amgen (BSR #42:  
Obesity) presented clinical data at the 
American Society of Hematology, that 
Aranesp appeared to be effective 
given just once every three weeks to 
anemic cancer patients with solid tu-
BioTech Sage Report, January 2001 
BioTech Stock Updates 
This section is to update and inform our readers 
on the status of those stocks that are in our Bio-
Portfolio.