Nanoforming the future of medicine
Management Presentation
November 18th, 2020
Nanoform is an innovative nanoparticle medicine enabling company with headquarters in Helsinki, Finland. The Company's patented and scalable Controlled Expansion of Supercritical Solutions (CESS®) technology produces nanoformed API particles as small as 10nm. This enables poorly soluble molecules in the pharmaceutical pipeline to progress into clinical development by increasing their rate of dissolution and by improving their bioavailability. Nanoform's share is listed on the Premier-segment of Nasdaq First North Growth Market in Helsinki (ticker: NANOFH) and Stockholm (ticker: NANOFS). Nanoform is researched by SEB, Danske Bank, Kepler Cheuvreux and Stifel. www.nanoform.com
Introduction to Nanoform
CEO Edward Hæggström
The structural pharma R&D problem
Only 48 drugs approved in the US last year… | …while the global pharma industry R&D expenditure exceeds USD 180bn |
Annual number of novel drug approvals by FDA 2010-2019 | Global pharmaceutical R&D spending 2010-2024E (USDbn) |
Chemical | Biologics | ||||||||||||||||||||||
60 | 250 | ||||||||||||||||||||||
50 | 17 | 200 | 189 | 196 | 202 | 207 | 213 | ||||||||||||||||
179 | 182 | ||||||||||||||||||||||
40 | 12 | 12 | 10 | 160 | 168 | ||||||||||||||||||
145 | 150 | ||||||||||||||||||||||
150 | |||||||||||||||||||||||
6 | 11 | 137 | 136 | 138 | |||||||||||||||||||
129 | |||||||||||||||||||||||
30 | |||||||||||||||||||||||
6 | 2 | 100 | |||||||||||||||||||||
20 | 7 | 42 | 38 | ||||||||||||||||||||
6 | |||||||||||||||||||||||
33 | 33 | 34 | |||||||||||||||||||||
30 | |||||||||||||||||||||||
25 | 50 | ||||||||||||||||||||||
10 | 24 | ||||||||||||||||||||||
15 | 15 | ||||||||||||||||||||||
0 | 0 | ||||||||||||||||||||||
2010 | 2011 | 2012 | 2013 | 2014 | 2015 | 2016 | 2017 | 2018 | 2019 |
- A game changer in particle design is needed to improve R&D yield
Source: U.S. Food and Drug Administration (FDA), New Drug Therapy Approvals 2019 (Annual number of drugs approved); EvaluatePharma, World | 3 |
Preview 2019, Outlook to 2024 (Annual R&D spend) |
Low bioavailability is the key issue
Poor bioavailability and low efficacy most common reasons for drug failure
Reasons for drug failure in pre-clinical trials (share of molecules)
45% | |||||||||
40% | |||||||||
35% | |||||||||
30% | |||||||||
25% | |||||||||
20% | 39% | ||||||||
15% | 30% | ||||||||
10% | |||||||||
11% | |||||||||
5% | 10% | 10% | |||||||
0% | |||||||||
Poor | Low efficacy | High toxicity | Adverse effects | Others | |||||
bioavailability |
Majority of new drugs suffer from poor solubility | ||
Solubility | ||
High | Low | |
Class I1 | Class II1 | |
High | On market: 35% | On market: 30% |
New drugs: 5-10% | New drugs: 60-70% | |
Permeability | 70-90% | |
of new drugs | ||
are poorly | ||
soluble | ||
Low | Class III1 | Class IV1 |
On market: 25% | On market: 10% | |
New drugs: 5-10% | New drugs: 10-20% |
- Nanoform can enhance the pharma industry output by targeting poorly soluble drugs
Source: GlobalData 2009, Cutting Edge Water-based Nanotechnology in Drug Development (Reasons for drug failure); Nikolakakis & Partheniadis | 4 |
(2017), Self-Emulsifying Granules and Pellets: Composition and Formation Mechanisms for Instant or Controlled Release (Share of poorly soluble | |
drugs) |
1) Classification of drug substance according to Biopharmaceutics Classification System (BCS)
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Nanoform Finland plc published this content on 18 November 2020 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 18 November 2020 10:12:04 UTC