The Q1 report was in line with expectations, with a small beat on the operating loss. The cash position at end-Q1 was nearly SEK1bn. There was limited news on the delayed EU approval (waiting on a SAG meeting). Eisai recently guided for Leqembi sales of JPY56.5bn (year to March 2025), implying royalties to BioArctic of cSEK360m. We reiterate our BUY and SEK350 target price.
The Q4 report was a non-event as Leqembi royalties had already been published. We believe investors will continue to focus on the Leqembi launch trajectory; however, we believe BioArctic’s pipeline will come into greater focus with the approaching start of the phase IIa trial for exidavnemab in Parkinson’s disease. We reiterate our BUY but have lowered our target price to SEK350 (365).
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Q3 earnings were slightly below our estimate, as the milestone received from Eisai was less than we expected. We have adjusted our uptake trajectory for Leqembi to reflect the complex infrastructure needed to administer the drug (multiple MRIs and i.v. infusions) and have significantly reduced our short-term sales forecasts. Longer-term, we expect Leqembi to be a game-changer for Alzheimer’s patients. We reiterate our BUY, but have cut our target price to SEK365 (410).
The Q2 report was fairly undramatic, coming just after the most important event in the company’s history – full FDA approval of Leqembi. BioArctic is turning its sights to possible approval in Japan in September as well as a full launch in the US by its partner Eisai. The pipeline of new projects looks solid, although there was no more detail. We reiterate our BUY but have lowered our target price to SEK410 (430) on our view of a slower sales ramp-up.
The FDA announced on 6 July that it had converted the accelerated approval for Leqembi to a full approval. As a result, we expect the CMS to grant the drug full reimbursement under the condition that patients take part in a data registry for the real-world outcomes of treatment with Leqembi. We note that the FDA recommends patients to be typed for ApoE4 status prior to initiation of treatment and that there is a Boxed Warning added to the label. We do not see this as something that should negati...
A director at I.A.R. Systems Group bought 60,000 shares at 81.500SEK and the significance rating of the trade was 69/100. Is that information sufficient for you to make an investment decision? This report gives details of those trades and adds context and analysis to them such that you can judge whether these trading decisions are ones worth following. Included in the report is a detailed share price chart which plots discretionary trades by all the company's directors over the last two years ...
The FDA advisory committee (AdCom) voted unanimously that the Clarity AD trial data confirmed the clinical benefit of Leqembi for the treatment of Alzheimer’s disease. The discussions in the panel circled around safety and the use of Leqembi in ApoE4 homozygotes and use in combination with anti-coagulant treatment. We believe the FDA will give full approval for Leqembi on 6 July and thus the drug should receive full reimbursement from the CMS soon after full approval.
The Q1 earnings beat was driven by EUR35m in milestones for initial US approval of Leqembi (substance name lecanemab) and filing in Europe and Japan. The next key event in our view is the PDUFA date (6 July), when we expect full FDA approval of Leqembi in the US. We reiterate our BUY and SEK430 target price.
The Q1 earnings beat was driven by EUR35m in milestones for initial US approval of Leqembi (substance name lecanemab) and filing in Europe and Japan. The next key event in our view is the PDUFA date (6 July), when we expect full FDA approval of Leqembi in the US. We reiterate our BUY and SEK430 target price.
The Q4 report was largely a non-event, as the share price is being driven by the regulatory and clinical development of lecanemab. The next important event looks to be the file acceptance message from the FDA and PDUFA date for the full approval application. This should come around 6 March and we expect a priority review (suggesting a PDUFA date around 6 September for a 6-month review process). We reiterate our BUY and SEK430 target price.
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