Calliditas Q1 report, January - March 2024
Rhea-AI Summary
Calliditas Therapeutics reported significant growth in Q1 2024 compared to Q1 2023. Net sales increased to SEK 295.5 million, with TARPEYO® contributing SEK 278.3 million. The company faced an operating loss of SEK 203.8 million and a loss per share of SEK 4.59. Cash reserves decreased to SEK 810.3 million from SEK 1,013.6 million. Key achievements include a 27% increase in enrollments, a new TARPEYO patent valid until 2043, and FDA's orphan drug exclusivity until 2030. Despite a USD 4.7 million revenue impact due to a cyberattack, future revenue is expected to remain stable. Upcoming events include European Commission decisions and Phase 2 trial results.
Positive
- Net sales increased to SEK 295.5 million in Q1 2024, up from SEK 191.4 million in Q1 2023.
- TARPEYO® net sales grew to SEK 278.3 million from SEK 185.7 million year-over-year.
- Record quarter with 705 enrollments, a 27% increase over Q4.
- New patent for TARPEYO valid until 2043 was issued by USPTO.
- FDA granted a seven-year orphan drug exclusivity for TARPEYO until December 2030.
- Positive preliminary net sales for Q2 amounting to USD 25.5 million.
- Positive results from Nefecon Phase 3 extension trial and setanaxib Phase 2 trial.
- Commercial launch of Nefecon in China by partner Everest Medicines.
Negative
- Operating loss increased to SEK 203.8 million in Q1 2024 from SEK 180.1 million in Q1 2023.
- Loss per share rose to SEK 4.59 from SEK 3.49 year-over-year.
- Cash reserves decreased to SEK 810.3 million from SEK 1,013.6 million as of March 31, 2024.
- Negative impact on TARPEYO revenues by approximately USD 4.7 million due to a cyberattack.
News Market Reaction 1 Alert
On the day this news was published, CALTX declined NaN%, reflecting a moderate negative market reaction.
Data tracked by StockTitan Argus on the day of publication.
Target market expansion following full approval in the US
JANUARY - MARCH 2024 (COMPARED TO JANUARY - MARCH 2023)
- Net sales amounted to
SEK 295.5 million , of which TARPEYO® net sales amounted toSEK 278.3 million , for the three months ended March 31, 2024. For the three months ended March 31, 2023, net sales amounted toSEK 191.4 million , of which TARPEYO net sales amounted toSEK 185.7 million . - Operating loss amounted to
SEK 203.8 million andSEK 180.1 million for the three months ended March 31, 2024, and 2023, respectively. - Loss per share before and after dilution amounted to
SEK 4.59 andSEK 3.49 for the three months ended March 31, 2024, and 2023, respectively. - Cash amounted to
SEK 810.3 million andSEK 1,013.6 million as of March 31, 2024, and 2023, respectively.
"In Q1 we generated another record quarter in terms of demand with 705 enrollments and 354 new prescribers. We are very excited over this positive trend, and we continue to see strong demand in Q2." - CEO Renée Aguiar-Lucander.
KEY TAKEAWAYS FROM Q1, 2024
- Calliditas had a record quarter with 705 enrollments, representing a
27% increase over Q4. - In February, the United States Patent and Trademark Office (USPTO) issued patent no. 11896719, entitled "New Pharmaceutical Compositions". This was Calliditas' second patent for TARPEYO in
the United States and provides product protection until 2043. - In March, the FDA granted an orphan drug exclusivity period of seven years for TARPEYO®, expiring in December 2030, based on when the company obtained full approval with a new indication for this drug product.
- There was a negative impact on net TARPEYO revenues in the quarter of approximately
USD 4.7 million due to a cyberattack on Change Health. The revenues we were not able to record in Q1 because of this technical issue are not lost, but are expected to roll forward over the next several months. This is not expected to have any impact on annual revenues.
KEY EVENTS AFTER THE REPORTING PERIOD
- Preliminary net sales from TARPEYO for the second quarter to date amounts to
USD 25.5 million . - Positive read out of the Nefecon Open label Phase 3 extension trial.
- Positive topline results from the setanaxib Phase 2 trial in head and neck cancer.
- Commercial launch of Nefecon in
China by partner Everest Medicines.
KEY EVENTS UPCOMING 6 MONTHS
- European Commission decision regarding a potential full approval for Kinpeygo for Calliditas' partner STADA.
- Full data read out of Phase 2 trial in Primary Biliary Cholangitis.
- Updated KDIGO guidelines expected in 2024.
Outlook for 2024: Unchanged
Calliditas expects continued revenue growth:
Total net sales from the Nefecon franchise, including milestones, are estimated to be
Investor Presentation:
May 23, 2024 14:30 CET
Link to webcast: Calliditas Therapeutics Q1 Report 2024 (financialhearings.com)
To participate via conference call register via this link: Call Access (financialhearings.com)
For further information, please contact:
Åsa Hillsten, Head of IR & Sustainability, Calliditas
Tel.: +46 76 403 35 43, Email: asa.hillsten@calliditas.com
The information in the report is information that Calliditas is obliged to make public pursuant to the EU Market Abuse Regulation. The information was sent for publication, through the agency of the contact person set out above, on May 23, 2024, at 7:00 a.m. CET.
This information was brought to you by Cision http://news.cision.com
The following files are available for download:
Q1 2024 Calliditas ENG | |
https://mb.cision.com/Public/16574/3986496/8e28fb584e477801.pdf | Q1 Press Release - ENG |
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SOURCE Calliditas Therapeutics