This is an article from Ingenious number 1, 2020.

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Interview with CEO Jan Nilsson

Mar 23, 2020

2019 was an eventful year for CombiGene, what do you feel are the most significant changes in CombiGene this year, as compared to a year ago?

We’ve brought the company forward considerably over the past year and, in my eyes, CombiGene is a completely different company than it was one year ago. Perhaps the most notable difference is that we are now focussing not solely on epilepsy. Our project portfolio has been broadened with a promising gene therapy project in the area of metabolic disorders, where today’s treatments are insufficient and extremely costly. Another important difference, which may not have received as much attention, is that we are now on our way to conclude the extensive development work surrounding our manufacturing method for CG01, and we have reached agreements with manufacturers. Everyone who works with gene therapy is well aware of the challenge manufacturing poses, and the fact that we have reached this stage adds considerable value in our discussions with potential collaborative partners.

You mention in the year-end statement that CombiGene has taken important steps forward where partnering is concerned. Can you elaborate on that?
It is always difficult to provide information about our partnering efforts, since we only want to give the market significant information without the risk of misinterpretation or pure speculation. Over the past year we have had several successful meetings with pharmaceutical companies, in both the largest category (Big Pharma) and with niched companies (Speciality Pharma), based mainly on interest in our candidate drug, CG01. These types of discussions always take place over a longer period. As a rule, initial contacts are characterized by tentative information exchange, and updates are often given in conjunction with larger partnering conferences (e.g., BioEurope). During subsequent stages information is exchanged in accordance with confidentiality agreements. Here, results from study reports are discussed and meetings with the scientific teams are held. The subsequent process varies depending on who the counterpart is, but typically involves access to a data room, question-and-answer rounds (scientific, commercial, regulatory and due diligence) and dialogues concerning the terms of possible commercial collaboration. In some cases, the counterpart wants to see certain data before making a decision. Several of these types of dialogues have taken place during 2019 and are ongoing, but to avoid misunderstanding, we have chosen not to share any specific information about our current status in this regard. Partnering dialogues usually take place over a period of several years and have a lot to do with building trust and credibility on the part of both parties, not only in terms of data but also in terms of the people who work within the company, which is an important consideration for a partner.

CombiGene announced on February 18th that the company intends to carry out a rights issue. Had you foreseen that the market would react negatively?
CombiGene is a development company with no revenue, so I don’t think it came as a surprise for our owners that the company needs additional funding in order to carry our projects forward. We have carried out new issues before and are aware that this usually results in a decline in the share price. This time, other factors are coming into play, primarily, the coronavirus outbreak, which is having a negative impact on many markets. It is always difficult to predict how the market will react. We are therefore trying to focus on long-term value creation by delivering on our development plan.

What is CombiGene’s strategy for establishing the terms for an issue?
Since it is important that we identify collaborative partners who believe in CombiGene and on whom we can rely, we normally procure an advisor prior to each new capital acquisition. In each financing round, the aim is always to raise the capital we need at the best possible terms for our shareholders. Finding ’the best possible terms’ is more difficult than one might think and we must get used to the fact that, unfortunately, it is impossible to satisfy all shareholders. People in the management and the board are also shareholders, which makes it natural to try to find a good balance. Usually, the first decision to make is what discount to offer on the share price to create an incentive for subscribing without diminishing the value for our existing shareholders. This can be difficult since, as a company, it is hard to influence your market capitalization at the point in time when a capital requirement arises. To minimize dilution, it is therefore logical to design a funding strategy whereby warrants can be converted at future points in time when the company has reached development milestones and increased in value. Similarly, investors in development companies normally opt to inject capital at intervals, instead of making a single large investment. Finally, we have seen that guaranteed issues have a greater probability of attracting interest, so this is usually a safe way of ensuring that the target for the issue is reached.

What would you like to say to shareholders who are concerned about CombiGene’s current market cap?
Of course, I think that the situation is regrettable. It is completely reasonable to worry when the share price is lower than the acquisition value. The share price is beyond my control and I hope that our shareholders feel confident when they consider how CombiGene has developed during my years as CEO. As I mentioned earlier, our CG01 development programme has made very considerable progress and our portfolio has been broadened in the past year to include another project. These activities create value for the company and should eventually result in increased shareholder value.

How would you describe the motives for the issue?
The purpose of the issue is to secure resources to drive our epilepsy project, CG01, forward with full force. Results from animal studies and studies by our scientific founders on NPY in donated human brain tissue show very promising potential. Most of the funds raised from the issue will be used to produce CG01 material, which will enable us to conduct the safety and biodistribution studies before we can start the first clinical study.

What is the time horizon for these activities?
During 2020 we will also use the material to be able to conduct studies to determine how best to administer CG01 to the human brain. During 2021 we plan to carry out the safety studies (biodistribution and toxicology) that are necessary to obtain authorization from regulatory authorities to conduct studies in humans. The safety studies will take about six months, after which it will take about a further six months to analyse the results. Concurrently, we are also making preparations for the start of the clinical study. For example, we will design the study, meet with the regulatory authorities and discuss our project with the clinics that have expressed interest in conducting the clinical study.

When do you think the first study in humans will begin?
There is always a degree of uncertainty when a new therapy is developed, but as soon as we have the final report from the safety studies, our plan and ambition is to submit an application to the regulatory authorities for authorization to start the first human study.

That sounds very exciting.
It certainly is. To have the opportunity to work with a project that can ultimately help people is very gratifying. However, as with all drug development, it is very time consuming and resource intensive. There are many significant milestones along the way, but one of the most important is the start of the first clinical study. In my experience, it is also one of the milestones when you can really see a marked increase in value in the project.

Many gene-therapy projects, both those which have reached the market and those which are still under development, are aimed at very rare diseases. This is not the case with CG01.
Precisely. CG01 will address a very big target group. In the USA alone some 14,000 patients are diagnosed with drug-resistant focal epilepsy each year. Realistically, 10-20 percent of these patients could be treated with CG01 and even a conservative estimate places the market potential for CG01 at 4-10 billion kronor per year. Our lipodystrophy project is different in the sense that it is aimed at a rare patient group for which the majority of patients now lack a satisfactory treatment. The current treatment for lipodystrophy, Myalept, can unfortunetly not help the subpopulation we aim to help. Myalept is without exception the most expensive drug in the USA, which shows that there is a very high degree of willingness to pay for treatment of lipodystrophy.

How long will funds from the issue last?
The further you proceed with a drug development project, the more it costs. Funding from the ongoing issue will mean that we can drive CG01 with full force through 2020. That horizon is appropriate, since it will allow us to reach a number of important milestones, which we feel makes the offer attractive for our existing shareholders and new investors in this issue. Thereafter, we will need additional capital.

Will this mean another rights issue during 2021?
It’s too soon to say. A rights issues is one of several alternatives. We also have the option of applying  for other types of grants, just as we did, successfully, with Horizon 2020. A directed share issue is also plausible, or we may by then have found a strong investment partner. For the time being, I am not discounting any alternatives. I wish to add that we are working continuously on several fronts to secure long-term funding for our projects. This effort includes all of the alternatives I mentioned above.

Am I right in understanding that the funds from the ongoing issue will primarily be used in the CG01 project and not the lipodystrophy project?
That is correct. The reason is that CG01 has come a lot farther development-wise and therefore costs more, precisely as I explained earlier. However, our level of ambition for the lipodystrophy project remains high. The project is off to a very good start and we are managing it exactly as planned, but since the project is still in an early stage of development, it is not as costly as CG01.

 

 

CombiGene’s lead project CG01 has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 823282

About CombiGene

CombiGene’s vision is to provide patients affected by severe life-altering diseases with the prospect of a better life through novel gene therapies. CombiGene’s business concept is to develop effective gene therapies for severe life-altering diseases where adequate treatment is currently lacking. Development assets are sourced from an external research network and developed to achieve clinical proof of concept. Drug candidates for common diseases will be co-developed and commercialized through strategic partnerships, while the company may manage this process on its own for drugs targeting niched patient populations. The company is public and listed on the Swedish marketplace Nasdaq First North Growth Market and the company’s Certified Advisor is FNCA Sweden AB, +46 (0)852 80 03 99 info@fnca.se.

 

Combigene AB, Medicon Village, SE-223-81 Lund, Visiting adress: Scheelevägen 2, Lund, Sweden

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