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Allakos Inc
Tax Provision
Allakos Inc
Tax Provision Peer Comparison
Competitors Analysis
Latest Figures & CAGR of Competitors
Company | Tax Provision | CAGR 3Y | CAGR 5Y | CAGR 10Y | ||
---|---|---|---|---|---|---|
Allakos Inc
NASDAQ:ALLK
|
Tax Provision
N/A
|
CAGR 3-Years
N/A
|
CAGR 5-Years
N/A
|
CAGR 10-Years
N/A
|
||
Abbvie Inc
NYSE:ABBV
|
Tax Provision
-$2.1B
|
CAGR 3-Years
N/A
|
CAGR 5-Years
N/A
|
CAGR 10-Years
-6%
|
||
Gilead Sciences Inc
NASDAQ:GILD
|
Tax Provision
-$63m
|
CAGR 3-Years
68%
|
CAGR 5-Years
48%
|
CAGR 10-Years
30%
|
||
Amgen Inc
NASDAQ:AMGN
|
Tax Provision
-$449m
|
CAGR 3-Years
19%
|
CAGR 5-Years
19%
|
CAGR 10-Years
0%
|
||
Vertex Pharmaceuticals Inc
NASDAQ:VRTX
|
Tax Provision
-$739.4m
|
CAGR 3-Years
-9%
|
CAGR 5-Years
-31%
|
CAGR 10-Years
-61%
|
||
Regeneron Pharmaceuticals Inc
NASDAQ:REGN
|
Tax Provision
-$314.9m
|
CAGR 3-Years
33%
|
CAGR 5-Years
-20%
|
CAGR 10-Years
3%
|
Allakos Inc
Glance View
Allakos, Inc. engages in the development of therapeutic antibodies. The company is headquartered in Redwood City, California and currently employs 192 full-time employees. The company went IPO on 2018-07-19. The firm is developing therapeutics, which target immunomodulatory receptors present on immune effector cells involved in allergy, inflammatory, and proliferative diseases. Its advanced antibodies are lirentelimab (AK002) and AK006. AK002 selectively targets both mast cells and eosinophils, two types of white blood cells that are widely distributed in the body and play a central role in the inflammatory response. The company is developing AK002 for the treatment of eosinophilic esophagitis (EoE), eosinophilic gastritis (EG), eosinophilic duodenitis (EoD), atopic dermatitis, chronic spontaneous urticaria and additional indications. AK006 targets Siglec-6, an inhibitory receptor expressed selectively on mast cells. The company also developed a formulation of lirentelimab for subcutaneous (SC) administration. The firm is also developing additional antibodies targeting inhibitory receptors expressed on key disease-driving immune cells.