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Marinomed Biotech AG (MARI-AT): Solving the insoluble

Dow Jones received a payment from EQS/DGAP to publish this press release.

goetzpartners securities Limited 
Marinomed Biotech AG (MARI-AT): Solving the insoluble 
 
21-March-2019 / 08:15 GMT/BST 
 
*Free to access research and investor meetings in a post-MiFID2 world.* 
 
*This research report is intended for use only by persons who qualify as 
professional investors or eligible counterparties (institutional investors) in 
the applicable jurisdiction, and not by any private individuals or other 
persons who qualify as retail clients.* 
 
*Published to the market and investors on 21st March 2019 @ 7.48am (GMT).* 
 
*Marinomed Biotech AG (MARI-AT): Solving the insoluble* 
*Recommendation: OUTPERFORM* 
*Target Price: EUR95.00 * 
*Current Price: EUR78.00 (CoB on 20th March 2019) * 
 
*KEY TAKEAWAY* 
 
We initiate coverage of Marinomed Biotech AG ("MARI") with an OUTPERFORM 
recommendation and a target price ("TP") of EUR95 per share (>20% upside). 
Marinomed uses its proprietary Marinosolv technology to dissolve hardly 
soluble therapeutic compounds to improve their bioavailability and hence 
efficacy and safety. Pivotal Phase III data for lead asset Budesolv in hay 
fever (allergic rhinitis, "AR") is expected in Q2/2019E, paving the way for 
approval and launch in 2021E into a >$12.2bn market. We model peak sales of 
EUR750m (<4% market share), with Marinomed retaining up to 16% of value 
through distribution deals. Tacrosolv is due to enter Phase II for eye 
diseases in 2019E. Marinomed already generates revenues from six marketed over 
the counter ("OTC") products for cough and colds, discovered and developed 
in-house based on the patented and clinically validated Carragelose platform. 
 
*Budesolv Phase III data in allergic rhinitis in Q2/2019E the key catalyst* 
 
Budesolv contains the steroid budesonide, used for allergy and autoimmune 
diseases. It is being developed as a nasal spray for AR, an inflammation of 
the nasal mucous membranes that affects up to 30% of people. The ongoing Phase 
III trial is designed to show non-inferiority vs. Johnson & Johnson's OTC 
product Rhinocort Aqua (budesonide suspension), which generated sales of $250m 
in 2017, less than 2 years after the Rx-to-OTC switch. Marinomed plans to 
differentiate Budesolv based on faster onset of relief - minutes rather than 
days - through a secondary endpoint. This would position it as a competitor to 
market leader Flonase, which had sales of c.$1.6bn in 2017. 
 
*Tacrosolv is targeted at common and debilitating, yet underserved eye 
diseases* 
 
Tacrosolv is based on tacrolimus, an established immunosuppressant used in 
organ transplantation. Marinomed intends to develop the compound as a 
prescription drug for local application to the eye to treat allergic 
conjunctivitis and dry eye syndrome. The addressable markets were c.$1.4bn and 
c.$2.2bn, respectively, in 2017. Preclinical studies have demonstrated 
excellent tissue permeation and bioavailability at doses well below those used 
when tacrolimus is administered systemically. A Phase II challenge study in 
allergic conjunctivitis is due to start in 2019E, paving the way for pivotal 
Phase III studies in 2020E. We expect Marinomed to partner Tacrosolv after 
Phase II in a EUR500m deal including 12.5% royalties on sales and model peak 
sales of EUR1bn, of which dry eye accounts for 75%. 
 
*Marketed Carragelose-based products target a c.$28bn OTC market* 
 
The efficacy of Carragelose, which is based on a biopolymer with antiviral 
properties, has been demonstrated in four clinical trials in 650 adults and 
children, which showed a reduction in the duration of the cold (by 2 - 3 
days), its symptoms, and the number of relapses. Marinomed has six Carragelose 
products targeting the cough, cold and allergy ("CCA") market worth c.$28bn in 
2017 and growing at 4% - 5% per year. They are marketed through partners 
worldwide and generated sales between EUR28m - EUR43m in 2017, yielding 
EUR4.8m in total revenue to Marinomed. We forecast peak sales of c.EUR260m in 
2030E (<1% market share) - with Marinomed entitled to c.16% - driven by 
continued growth of existing products in markets where they are already 
launched, entry into new countries that are covered by existing partnerships 
and launch of new products. 
 
*TP of EUR95 per share suggests >20% upside* 
 
Marinomed develops products based on two proprietary platforms (OTC medicines 
and new, aqueous formulations of existing drugs) that have distinct risk / 
reward profiles. We feel that the valuation methodology that best captures 
their different risk / reward profiles as well as their long-term potential is 
a sum-of-the-parts ("SoTP") analysis based on risk-adjusted net present values 
("rNPVs") for Carragelose products and projects from the Marinosolv technology 
platform. The most valuable asset is Budesolv, accounting for c.43% of our 
valuation, followed by Carragelose products (31%). Positive data for Budesolv 
in Q2/2019E would lift our valuation to EUR107 per share. 
 
Kind regards, 
 
Brigitte de Lima | Analyst 
 
goetzpartners Healthcare Research Team | Research Team 
 
goetzpartners securities Limited 
 
The Stanley Building, 7 Pancras Square, London, N1C 4AG, England, UK. 
 
T +44 (0) 203 859 7725 | brigitte.delima@goetzpartners.com / 
healthcareresearch@goetzpartners.com 
 
www.goetzpartnerssecurities.com [1] 
 
goetzpartners securities LinkedIn page [2] 
 
Registered in England No. 04684144. 
 
Managing Directors: Dr Stephan Goetz, Martin Brunninger and Ulrich Kinzel. 
 
*goetzpartners securities Limited - Team Members* 
 
Equity Research Analysts - Martin Brunninger, Brigitte de Lima, Chris Redhead 
and Martin Piehlmeier. 
 
Sales / Marketing - Erland Sternby. 
 
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790119 21-March-2019 
 
 
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(END) Dow Jones Newswires

March 21, 2019 04:15 ET (08:15 GMT)

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