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Last kr10.60 SEK
Change Today -0.25 / -2.30%
Volume 743.9K
ACTI On Other Exchanges
Symbol
Exchange
Stuttgart
Stockholm
OTC US
OTC US
As of 11:30 AM 05/29/15 All times are local (Market data is delayed by at least 15 minutes).

active biotech ab (ACTI) Snapshot

Open
kr10.90
Previous Close
kr10.85
Day High
kr11.10
Day Low
kr10.60
52 Week High
08/14/14 - kr33.60
52 Week Low
04/16/15 - kr8.55
Market Cap
953.0M
Average Volume 10 Days
94.9K
EPS TTM
kr-2.81
Shares Outstanding
89.9M
EX-Date
02/15/01
P/E TM
--
Dividend
--
Dividend Yield
--
Current Stock Chart for ACTIVE BIOTECH AB (ACTI)

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active biotech ab (ACTI) Details

Active Biotech AB (publ) develops drugs for the treatment of neurodegenerative diseases and cancer. The company has two projects in clinical development, such as laquinimod and tasquinimod. The Laquinimod project is a novel immunomodulatory compound for the treatment of neurodegenerative diseases; and the Tasquinimod project is an immunomodulatory, anti-metastatic substance for the treatment of prostate cancer. The company is also developing Paquinimod, an oral immunomodulatory compound for the treatment of systemic sclerosis; and RhuDex, an orally active compound for the treatment of autoimmune diseases. Its preclinical project product is ISI–Inhibition of S100 Interactions for producing patentable chemical compounds that interact with one of the quinoline compounds’ target molecules. Active Biotech AB (publ) is headquartered in Lund, Sweden.

56 Employees
Last Reported Date: 04/23/15

active biotech ab (ACTI) Top Compensated Officers

Chief Executive Officer and President
Total Annual Compensation: kr5.0M
Compensation as of Fiscal Year 2013.

active biotech ab (ACTI) Key Developments

Teva Pharmaceutical Industries Ltd. and Active Biotech Announce First Patient Enrolled in Phase II Study Evaluating Laquinimod for Primary Progressive MS

Teva Pharmaceutical Industries Ltd. and Active Biotech announced the first patient has been enrolled in the study ARandomized Placebo-controlled Trial Evaluating Laquinimod in PPMS, Gauging Gradations In MRI and Clinical Outcomes, a Phase II study to evaluate laquinimod, an investigational, oral, immune modulator, for the treatment of primary progressive multiple sclerosis. Currently there are no approved treatments for PPMS, representing a condition with a high unmet need. PPMS affects approximately 15% of all MS patients and is characterized by the worsening of neurologic function without distinct relapses. Unlike patients with relapsing-remitting MS, those with PPMS tend to have more lesions in the spinal cord than in the brain and these brain lesions usually contain fewer inflammatory cells. In addition, all studies evaluating RRMS treatments in patients with PPMS have failed to prove effective for this condition. ARPEGGIO is a multinational, multicenter, randomized, double-blind, parallel-group, placebo-controlled study of once-daily, oral laquinimod in patients with PPMS. The study’s primary endpoint is percent brain volume change through MRI analysis. The trial will enroll approximately 375 patients in the U.S., Canada, and Europe. Additional details on the study design will be presented at the AAN Annual Meeting in Washington, D.C. on April 23, 2015 during Poster Session 7.

Active Biotech AB Reports Earnings Results for the First Quarter of 2015

Active Biotech AB reported earnings results for the first quarter of 2015. For the quarter, the company reported net sales of SEK 2.9 million against SEK 2.1 million a year ago. Operating loss was SEK 57.4 million against SEK 29.2 million a year ago. Loss for the period was SEK 58.0 million or SEK 0.64 per share against SEK 60.2 million or SEK 0.80 per share a year ago.

Active Biotech and Ipsen Announce Top Line Results of the 10TASQ10 Study

Active Biotech and Ipsen announced top line results of the 10TASQ10 study. While the study showed that tasquinimod reduced the risk of radiographic cancer progression or death compared to placebo (rPFS, HR=0.69, CI 95%: 0.60 0.80) in patients with metastatic castration resistant prostate cancer (mCRPC) who have not received chemotherapy, tasquinimod did not extend overall survival. Efficacy results together with preliminary safety data do not support positive benefit risk balance in this population. Therefore the companies have decided to discontinue all studies in prostate cancer. Full results will be presented at an upcoming scientific conference. The outcome of the 10TASQ10 study is a major disappointment based on the promising phase II results. However, the data at hand is unambiguous and cannot motivate further development of tasquinimod in this patient population.

 

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Valuation ACTI Industry Range
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Price/Sales 88.7x
Price/Book 2.8x
Price/Cash Flow NM Not Meaningful
TEV/Sales 44.9x
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