Investor Presentation • Dec 3, 2020
Investor Presentation
Open in ViewerOpens in native device viewer



This presentation (the "Presentation") is for informational purposes only and do not constitute an offer to sell, a solicitation of an offer to buy, or a recommendation to purchase any equity, debt or other financial instruments of Canndoc Ltd. ("Canndoc") or InterCure Ltd. ("InterCure"). The information contained herein does not purport to be all-inclusive. The data contained herein is derived from various internal and external sources. No representation is made as to the reasonableness of the assumptions made within or the accuracy or completeness of any projections, modeling or any other information contained herein. Any person at any time acquiring securities must do so only on the basis of such person's own judgment as to the merits or the suitability of the securities for its purpose and only based on such information as is contained in such public filings, after having taken all such professional or other advice as it considers necessary or appropriate in the circumstances and not in reliance on the information contained in the Presentation. Canndoc and InterCure assume no obligation to update the information in this Presentation. Neither Canndoc nor InterCure accepts any liability whatsoever for any losses arising from the use of this Presentation or reliance on the information contained herein. Nothing herein shall be deemed to constitute investment, legal, tax, financial, accounting or other advice. Historical facts and past operating results are not intended to mean that future performances or results for any period will necessarily match or exceed those of any prior year.
This Presentation contains forward-looking statements that involve substantial risks and uncertainties. All statements, other than statements of historical facts, included in this presentation are forward-looking statements within the meaning of the Israeli Securities Law, 1968. Such forward looking statements with respect to strategies, prospects and other aspects of the businesses of Canndoc are based on current expectations that are subject to risks and uncertainties. Various important factors could cause actual results or events to differ materially from those that may be expressed or implied by the forward-looking statements, including without limitation, changes in the regulation and climate, the impact of the COVID-19 pandemic and changes in the market conditions. The forward-looking statements are made as of this date and Canndoc or InterCure do not undertake any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

Leading the global Pharma grade cannabis industry through our commitment to quality, innovation and improving lives.


5 Operating territories and establishing partnerships in key target markes

10 IMCA approved advanced clinical trials

13 Years of experience and unique knowhow

40+ Thousands of patients treated with CANNDOC'S medical cannabis products over the years

32 Tones of GMP medical cannabis products under long term agreements

100 100% of the Authorized Pharmacies in Israel selling CANNDOC'S GMP products

100+ Scalable International supply chain for 100+ Tons of high quality GMP production
140 / 85 / 31% MKT CAP 140M\$ [TASE:INCR] Capital 85M\$ EBITDA 31% + POSITIVE CF
-

Pharma grade (GMP)
Medical/recreational


Source: Market research companies













aphria" E ORGANIGRAM &TILRAY
t.ookies



Total of 1,300,000 square feet
Max capacity of 140 tons annually

Total of 560,000 square feet
Max capacity of 70 tons annually



Total of 350,00 square feet
Max capacity of 25 tons annually
‣ ‣ ‣ Ability to significantly scale up cultivation operations without capital investment


‣ ‣ Established global footprint representing ~1B\$ of cultivation facility investment
‣ Intercontinental supply chain for consistent and highest quality branded products for all addressable markets



Brands
Licensed producers







COUCBOM INCREA THC20/CEDA INCICA

CANBOCES
10g ====
ATILRAY


0
10g Park Party































First Israeli LP to become a public company
First Israeli company to import medical grade cannabis into Israel
First to receive export approval to Europe















‣ Double-blind, randomized, placebo-controlled (1:1) ; Full spectrum derived cannabis oil
Change in median monthly seizure frequency over study period compared
Treatment-emergent adverse events and serious adverse events (SAEs) during treatment
| Phase of Development |
Indication | Number of Patients | Primary Endpoint(s) |
|---|---|---|---|
| 2a | Adult Epilepsy | 52 | - Change in median monthly seizure frequency over study period compared to 2-month baseline period |
| 2a | CINV related to Breast Cancer Treatment |
72 | - SAEs during treatment |
| 2a | Parkinson's Disease | 60 | - SAEs during treatment - Change in The Parkinson's Disease Questionnaire |
| 2a | Diabetic Neuropathy | 44 | - Neuropathic Pain Diagnostic Questionnaire score (scale 4-10) |
| 2a | Fibromyalgia | 62 | - Safety and tolerability of the product based on AEs during treatment - To determine the effect of the product on Fibromyalgia Impact Questionnaire |
| 2a | Rheumatoid Arthritis | 64 | - To determine the effect of the product on ACR20 |
| 2a | Radicular Pain | 36 | -Safety of the product |

Safety and tolerability of the product based on AEs during treatment - To determine the effect of the product on Fibromyalgia Impact Questionnaire - To determine the effect of the product on Physician Global Impression of Change
Safety and tolerability of the product based on Adverse Events during treatment - To determine the effect of the product on ACR20

‣ Double-blind, randomized, placebo-controlled (1:1) ; Full spectrum derived cannabis oil
- Characterize the effects of medicinal cannabis in different THC:CBD ratios on associated morbidity on the Autistic spectrum To examine the influence of cannabis treatment on cognitive and adjacent capabilities Test the levels of THC and CBD in children treated with cannabis
| Primary Endpoint(s) | Number of Patients | Indication | Phase of Development |
|---|---|---|---|
| on the Autistic spectrum | 75 | Pediatric/Young Adult Autism |
3 |
| Lumbar Radiculopathy | 50 | Lumbar Radiculopathy |
2a |
| - Safety rate of AEs - Improvement in Pittsburgh sleep quality index-addendum (PSQI-A) score |
50 | Post-Traumatic Stress Disorder |
2a * |
-Safety and tolerability of the product based on AEs during treatment -To evaluate the pain-relieving effect of CD-008 sublingual drops, in addition to standard of care, on

* Pending IMCA approval
















Deducting income and expenses that are not ordinary operations *




PHARMA GRADE LEADERSHIP




FOCUSED ON PROFITABLE GROWTH



Building tools?
Free accounts include 100 API calls/year for testing.
Have a question? We'll get back to you promptly.