Hansa Biopharma Interim Report January–June 2019
Highlights for the second quarter 2019
- At the 2019 American Transplant Congress (ATC), Dr. Edmund Huang of Cedars-Sinai Medical Center presented data demonstrating a significant reduction in time to transplant for highly sensitized patients treated with imlifidase over matched controls waiting under Kidney Allocations System (KAS). Dr. Huang’s session won ATC’s People’s Choice Award for the most impactful presentation.
- Hansa Biopharma continued to advance imlifidase toward potential marketing authorization for enabling kidney transplantation in highly sensitized patients in the EU and the U.S. MAA is currently under review by EMA while complementary analyses are conducted in the U.S. to further illustrate the value of imlifidase over matched controls. Subsequent meeting with the FDA expected to take place in the second half of 2019.
- CTA approvals received in Europe for a Phase 2 study with imlifidase in Guillain-Barré Syndrome (GBS). The initiation of the GBS study represents a continuation of the Company’s expansion outside the transplantation area into autoimmune diseases.
- Divested the equity holding in Genovis, which generated gross proceeds of SEK 89m (USD 9.6m).
- All resolutions passed at Hansa Biopharma’s 2019 Annual General Meeting. Two new board members, Eva Nilsagård and Mats Blom, appointed.
- Spending in R&D and SG&A increased in the second quarter to SEK 46m (Q2’18 SEK 44m) and SEK 39m (Q2’18 SEK 15m) respectively as the Company continues to ramp-up in R&D and prepare for a potential launch of imlifidase in kidney transplantation.
- Cash flow from operating activities for the second quarter ended at SEK -78m (SEK -49m); the Company’s cash position ended at SEK 763m end of June 2019. Cash flow was mainly driven by investments in activities related to the potential launch of imlifidase and the divestment of the Genovis equity holding.
|SEKm, unless otherwise stated||Q2 2019||Q2 2018||H1 2019||H1 2018|
|Other operating income/expenses||-0.1||-0.8||-1.2||-1.0|
|Cash flow from operating activities||-78.0||-49.0||-179.6||-93.1|
|Cash and short term investments June 30, 2019||762.7||534.2||762.7||534.2|
|Shareholders’ equity, June 30, 2019||755.4||543.0||755.4||543.0|
|EPS before and after dilution June 30, 2019 (SEK)||-2.06||-1.55||-3.87||-2.77|
|Number of outstanding shares, June 30, 2019||40,026,107||38,083,125||40,026,107||38,083,125|
|Weighted average number of shares before and after dilution||40,026,107||37,976,440||40,014,056||37,962,440|
|Number of employees, June 30, 2019||60||40||60||40|
Søren Tulstrup, President and CEO, comments
“Hansa Biopharma’s evolution into a commercial stage biopharmaceutical company continues according to plan. During the second quarter, our organization grew its footprint in both Europe and the U.S., and we continued to increase our engagement with the broader healthcare community within transplantation, autoimmune diseases and beyond.
I recently returned from the 2019 American Transplant Congress (ATC) in Boston where I noted a high level of excitement around Hansa Biopharma, our technology platform and our pipeline. Imlifidase was highlighted in three presentations during the conference including a plenary presentation by Dr. Edmund Huang from Cedars-Sinai Medical Center in Los Angeles. Dr. Huang presented data demonstrating that imlifidase significantly reduces the time to transplant for patients treated with imlifidase compared to matched controls on the kidney transplantation waitlist. This session won the ATC’s People’s Choice Award as the most impactful to the transplant community, further validating the transformative potential of imlifidase and our technology.
In the U.S., we are seeing signs from the current administration that increasing the kidney transplant rate and improving equity of access to this lifesaving therapy is high on the political agenda as part of a goal to significantly increase survival rate and quality of life for dialysis patients and at the same time reduce the > $100 billion spent annually by the U.S. government to treat chronic kidney disease and end-stage renal disease. If approved, imlifidase could be a key driver in helping thousands of highly sensitized patients get off of dialysis by enabling transplantation.
The regulatory review process for imlifidase in Europe is progressing following the acceptance of our Marketing Authorization Application (MAA) in February. The timeline for the process is 210 working days plus clock stops, as we have communicated earlier. Meanwhile, in the U.S. we are conducting complementary analyses with respect to transplantability for the highly sensitized patients participating in the Phase 2 studies with imlifidase compared to matched controls from the U.S. transplant registry in order to further illustrate the value of imlifidase in the U.S. healthcare system. Once completed, we will schedule a subsequent meeting with the U.S. Food and Drug Administration, which is expected to take place in the second half of 2019.
Overall, we continue to execute on our strategic agenda, with solid progress across our pipeline, including the recent initiation of two Phase 2 studies in Guillain-Barré Syndrome (GBS) and acute Antibody Mediated Rejection in kidney transplantation. In April, we decided to divest our equity holding in Genovis. The transaction provided a profitable exit from a non-core investment and generated funds that will help accelerate the development of our pipeline of clinical stage drug candidates as well as our next generation NiceR program for repeat dosing.
We envision a world where all patients with rare immunologic diseases can lead long and healthy lives. To help achieve this vision we are building a high-performance organization to exploit our unique immunomodulating technology platform to develop innovative lifesaving and life altering therapies, bring these to the patients with rare diseases who need them, and generate value to society at large.”
President and CEO of Hansa Biopharma
This is information that Hansa Biopharma AB is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of the contact person set out below at 08:00am CET on July 18, 2019.
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