SECOND QUARTER IN BRIEF
- Laquinimod eye drop phase I single ascending-dose part in healthy subjects was completed without reported safety concerns, multiple-dose part started
Active Biotech strengthened the patent protection for laquinimod in eye disorders (April 26 )- FDA granted Orphan Drug Designation for tasquinimod in myelofibrosis (
May 18 ) - Successful completion of the first stage of the phase IIa clinical study of naptumomab in combination with docetaxel, with the study now enrolling into the second stage (
June 1 )
EVENTS AFTER THE END OF THE PERIOD
- The first part of the multiple-dose of laquinimod eye drops in the phase I study has been completed without any serious side effects that can be linked to laquinimod and the study has been expanded with another dose group
- The board of directors resolved on
August 4, 2022 , based on the authorisation from the general meeting, to carry out a rights issue of approximatelySEK 55 million to secure financing of the ongoing and planned development programs
Financial summary
SEK M | Apr-Jun | Jan-Jun | Full-year | ||
2022 2021 | 2022 2021 | 2021 | |||
Net sales | - | - | - | - | - |
Operating profit/loss | -14,0 | -12,6 | -29,3 | -22,4 | -49,8 |
Profit/loss after tax | -14,3 | -12,6 | -30,0 | -22,4 | -49,8 |
Earnings per share (SEK) | -0,07 | -0,06 | -0,14 | -0,11 | -0,24 |
Cash and cash equivalents (at close of period) | 21,9 | 78,5 | 53,1 |
The report is also available at www.activebiotech.com.
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