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BREMNER
CAPITAL
MANAGEMENT
October 2014
Tekmira Pharmaceuticals Conference Calls
12/09/14
Participants:
Tekmira: Julie Rezler (IR), Mark Murray (CEO) and Bruce Cousins (CFO)
Bremner: Sam Kelly, Tancredi Marchiolo
Ebola update:
• The objective of the management is to get approval for their product
• The WHO are seeking to use RNA therapeutics to halt the spread of Ebola
• All parties are interested in and supportive of Tekmira's efforts
• for the TKM-Ebola product, the management see a narrow distribution model, mainly selling to
governments, with them being the distributors
• They also suggested that they may be seeking other commercial partners to distribute drugs that
they lack the capacity to distribute themselves
• The company is exploring a regulatory framework in which TKM-Ebola could be used anywhere in
the world
• When asked about testing of the drug on infected individuals the CEO said "our public information
states that we are only in the 1" phase of clinical trials", although his delivery and tone suggested
otherwise
1. They emphasised the importance of the other pipelines, besides TKM-Ebola
• The Hepatitis programme will go to the clinic next year and has strong commercialisation
potential
• They are seeking to expand their clinical oncology offering
2. Tekmira is, at least in the Ebola context, an arm of the US Government
• Their only concrete financial projections they made was a revenue stream of $70mn per
year from the US Department of Defence. They reached this figure by looking at the average
price the government pays for bio therapy drugs and multiplied it by the size of the stock
pile. However, both the estimated average price and the estimated stockpile were based on
the sentiment earlier this year. The management suggested that as the outbreak has spread,
both numbers could increase significantly —thus increasing the projected revenue streams
from the conservative $70mn/year
• When asked about demand from other governments or from the private sector, they did not
come up with any numbers. To me, this made it more certain that they will rely heavily on
the US government for revenue
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CAPITAL
MANAGEMENT
October 2014
• While the company was at pains to emphasise that they were free agents, operating without
restrictions from the US government, this was contradicted by two things a) they say they
are not testing the potentially life-saving drug on Ebola sufferers, and b) they will rely
heavily (if not solely) on the US government for revenues
• in addition, they made it clear that it was through government funding that they have
managed to scale up TKM-Ebola production capability to commercial levels
Our conclusions:
• The Ebola drug works
• Revenues from TKM-Ebola will be significantly higher than the $70mn/year estimate
• The company is operating under the wing of the US Government, this may slow the FDA approval
process
• There is a danger that the US government will keep TKM-Ebola on indefinite partial clinical hold, in
order to maintain the biowarfare competitive advantage that the vaccine imparts
• If the drug is sold commercially, the company will seek a large pharma partner to distribute it
• We should ride the waves of this stock, the management sounded like they were on the verge of
releasing very positive news: they were understated yet confident
UPDATE: Via email, we asked their investor relations representative whether they had provided TKM-Ebola to
the hospital treating the America Dr Rick Sacra. She did not reply until the end of the week and even then
failed to address my question directly. We took this as a sign that they were indeed using the treatment but
were not ready to release that information to the public. On the 22nd of September, Tekmira released a
statement confirming that the drug was being used to treat Or Sacra. In this statement, they also announced
that the FDA had authorised Tekmira to provide TKM-Ebola for treatment of infected patients under
expanded access protocols.
01/10/14
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CAPITAL
MANAGEMENT
October 2014
Participants:
Tekmira: Julie Rezler (IR)
Bremner: Sam Kelly
Q: As we discussed during the last call, we have fully supported your PR strategy thus far but we believe that
we have reached an important juncture. With the US seeing its first case of Ebola, and your drug being the
only one in the FDA approval pipeline, all eyes are on you. The news has piqued speculative interest and with
your shares up 28% in pre-market trading, there is an increased risk of significant volatility, unless the PR
adapts. As we see it, as holders of nearly 2% of your company, your actions in the next few days are vital for
reducing volatility and keeping shareholders on side. We would suggest releasing as much information as you
are permitted to, especially relating to the results of tests on infected patients and US government plans to
stockpile the drug.
A: We fully understand the importance of reduced volatility to investors, and we are keen to do all we can to
facilitate a reduction in volatility through our PR strategy. Should we temper the market by emphasizing that
TKM-Ebola has not completed clinical trials? Should we emphasise that the treatment was administered as
one of many clinical interventions, in the case of Dr Sacra?
Q: We feel that it is important to temper the market sentiment, however we wouldn't want you to be
unnecessarily negative. Any of the ideas above may be helpful to reduce volatility, but including positive news
along with that, perhaps from one of your other product pipelines, would help lessen the negative impact.
Could you perhaps release details of your work with the DoD in West Africa?
A: We are not currently using the treatment on anyone outside of the US. We appreciate the advice regarding
our PR strategy, it is always good to hear an investor's viewpoint.
UPDATE: Tekmira released a statement on the 2n° of October announcing that they had released a
development milestone in a project they are working on with Monsanto, prompting a $1.5mn payment. The
total value of the project, at completion, could reach $86.2mn.
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