![Page 1: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/1.jpg)
Developing Regenerative Therapies that Reverse Chronic Disease
David J. Mazzo, PhDPresident and Chief Executive Of f icer
August 13, 2020 | Nasdaq: CLBS
![Page 2: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/2.jpg)
This Investor Presentation contains forward-looking statements within the meaning of the PrivateSecurities Litigation Reform Act of 1995. Forward-looking statements reflect management’s currentexpectations, as of the date of this presentation, and involve certain risks and uncertainties. Allstatements other than statements of historical fact contained in this Investor Presentation areforward-looking statements. The Company’s actual results could differ materially from thoseanticipated in these forward-looking statements as a result of various factors. Factors that couldcause future results to differ materially from the recent results or those projected in forward-lookingstatements include the “Risk Factors” described in the Company’s Annual Report on Form 10-K filedwith the Securities and Exchange Commission (“SEC”) on March 5, 2020 and in the Company’s otherperiodic filings with the SEC. The Company’s further development is highly dependent on, amongother things, future medical and research developments and market acceptance, which are outside ofits control. You are cautioned not to place undue reliance on forward-looking statements, which speakonly as of the date of this Investor Presentation. Caladrius does not intend, and disclaims anyobligation, to update or revise any forward-looking information contained in this Investor Presentationor with respect to the matters described herein.
Forward-looking statement
2
![Page 3: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/3.jpg)
Investment case summary
Management team introduction
CD34+ cell therapy platform technology overview
Pipeline description and individual program summaries
Financial overview
Milestone timeline
Conclusion
Presentation contents
3
![Page 4: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/4.jpg)
CD34+ cell therapy company with an advanced clinical pipeline with 2 programs with “breakthrough” designation and 1 targeting COVID-19 induced lung repair
Proprietary field-leading technology in multi-billion dollar global indications backed by a strong IP portfolio
Multiple potential value creating events in the next 12-18 months based on milestones across the pipeline (timing subject to COVID-19 pandemic influence)
Seasoned management team with noteworthy domain expertise along withbig pharma and emerging biotech experience
Strong balance sheet; ~$42 million in cash & cash equivalents (July 31, 2020) with no debt and cash runway projected to fund operations through 2021
Caladrius investment rationale
4
![Page 5: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/5.jpg)
Note: Select experience is shown above. For a comprehensive bio, please visit: www.caladrius.com
Caladrius management team
5
David J. Mazzo, PhD President and
Chief Executive Officer
Douglas Losordo, MDEVP, Global Head of R&D and
Chief Medical Officer
Joseph Talamo, CPASenior VP and
Chief Financial Officer
Todd Girolamo, JDSenior VP, General Counsel
and Corporate Secretary
John MendittoVice President, IR and
Corporate Communications
![Page 6: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/6.jpg)
Ochsner Health, New OrleansDuke Clinical Research Institute
C. Michael Gibson, MDC. Noel Bairey Merz, MD Timothy Henry, MD
Thomas Povsic, MD, PhDScripps Clinic, San Diego
Richard Schatz, MD Christopher White, MD
Cedars-Sinai, Los Angeles Harvard Medical School The Christ Hospital, Cincinnati
Stanford Cardiovascular Institute
Joseph Wu, MD, PhDGoethe University, Frankfurt
Andreas Zeiher, MDUniversity of Florida, Gainesville
Carl Pepine, MD
Esteemed scientific advisory board
6
![Page 7: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/7.jpg)
CD34+ cell therapy platform technologyoverview
![Page 8: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/8.jpg)
Naturally occurring endothelial progenitor cells Reestablish blood flow to under-perfused tissues1,2
Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions3,4
1Mackie, A.R. et al., Tex Heart Inst J 2011, 38(5), 474-4852Kocher, A.A. et al., Nat Med 2001, 440-436
Normal microvasculature
Augmented microvasculature post-CD34+ cells treatmentCompromised microvasculature
Artery Vein
Capillaries
Artery Vein
Capillaries
Artery Vein
Capillaries
NewCapillaries
CD34+ cells have a well characterized mechanism of action
83Abd-Allah et al., Cytotherapy 2015, 17: 443-534Lo , B.C. et al., Am J Respir Cell Mol Biol 2017, 57: 651-61
![Page 9: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/9.jpg)
CD34+ cells have been studied clinically in a variety of ischemic disease indications by numerous investigators across many sites and countries
CD34+ cells repeatedly have shown evidence of vascular repair in multiple organs
Consistent and compelling results of rigorous clinical studies comprising >1,000 patients have been published in peer reviewed journals1-4
Single treatment has elicited durable therapeutic effect
No cell-related adverse events reported to date
1 Povsic, T. et al. JACC Cardiovasc Interv, 2016, 9 (15) 1576-15852 Losordo, D.W. et al. Circ Cardiovasc Interv, 2012; 5:821–830
3 Velagapudi P, et al, Cardiovas Revasc Med, 2018, 20(3):215-2194 Henry T.D., et al, European Heart Jour 2018, 2208–2216
CD34+ cell therapy is extensively studied/clinically validated
9
![Page 10: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/10.jpg)
Drug induced mobilization eliminates need for surgical bone marrow aspiration No genetic manipulation or ex vivo expansion of cells Four days or less from donation to treatment Cost-of-goods an order of magnitude less expensive than CAR-T therapies
Caladrius’ CD34 process is simple/fast/economical/scaled
Shipment
Day 1 Day 2 Day 3 or 4
Shipment
Sample collection via apheresis after CD34+ cell drug-induced mobilization
Isolation, concentration and formulation of CD34+/CXCR4+ cells
Cells returned to same patient by injection; site indication dependent
or
10
![Page 11: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/11.jpg)
U.S. patents granted
9 27Foreign patents
granted
Fundamental protection to 2031+
Key Claims Pharmaceutical composition of non-expanded CD34+/CXCR4+ stem cells Therapeutic concentration range Stabilizing serum Repair of injury caused by vascular insufficiency
Caladrius’ CD34 technology has robust intellectual property
11
![Page 12: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/12.jpg)
CLI = Critical Limb IschemiaCMD = Coronary Microvascular DysfunctionNORDA = No Option Refractory Disabling Angina
*Products are distinct and not interchangeable
Caladrius’ innovative CD34+ cell therapy pipeline*
12
1 Timing subject to COVID-19 pandemic influence
Product Indication Development Stage Commercialization Target1
mid-2022Registration eligible trial (Japan; ongoing)CLBS12 CLI
TBDPhase 3 confirmatory (USA; initiation pending funding)CLBS14 NORDA
TBDPhase 2b (USA; start target 4Q 2020)CLBS16 CMD
TBDPilot (USA; start target 3Q 2020)CLBS119 COVID-19 Lung Damage
![Page 13: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/13.jpg)
CLBS119COVID-19 Induced Lung
Damage(USA)
![Page 14: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/14.jpg)
Human coronavirus disease-19 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Evidence suggests1-3 that severe lung damage due to COVID-19 leads to long term disability and possibly death as a result of inflammation and vascular damage
Early data shows that almost all patients who survive COVID-19 pneumonia have some level of lung damage visible in CT scans taken before hospital discharge4
Prior data from the SARS epidemic suggest that CD34+ cells in the lung could be a target of SARS-CoV-2 infection and that destruction of lung CD34+ progenitors could account for the inability of patients with severe lung damage to recover fully5
Indication: COVID-19 induced lung damage
141 Varga Z, et al., Lancet. 2020;395(10234):1417‐14182 Lo., et al, Am J Respir Cell Mol Biol, 2017. 57(6): p. 651-6613 Abd-Allah SH., et al, Cytotherapy, 2015. 17(4): p. 443-453
4 Yuhui Wang, et al, Radiology, March 19, 20205 Chen Y, et al. J Exp Med. 2007;204(11):2529‐2536.
![Page 15: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/15.jpg)
The FDA has authorized Caladrius’ IND for the study of CLBS119, a CD34+ cell therapy for the repair of COVID-19 induced lung damage
CLBS119 will be studied in an open-label pilot clinical trial to evaluate the safety and efficacy of autologous peripheral blood derived CD34+ cells delivered by intravenous infusion
Safety endpoints include examination of adverse events, laboratory investigations, physical examinations, vital signs and occurrence of death
Efficacy endpoints include clinical measures such as oxygen saturation, supplemental oxygen requirement, pulmonary function testing and resolution of pulmonary infiltrates
Study initiation target: 3Q 2020
Our solution: CLBS119
15
![Page 16: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/16.jpg)
SAKIGAKE designated – Japan
Advanced Therapeutic Medicinal Product (ATMP) designated - EU
CLBS12Critical Limb Ischemia
(Japan)
![Page 17: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/17.jpg)
Severe arterial obstruction impeding blood flow in the lower extremities
Often found as a co-morbidity in diabetes patients
Includes severe rest pain and non-healing ulcers
Buerger’s disease (inflammation in small and medium arteries) a form of CLI associated with a history of heavy smoking
Patients with no-option CLI have persistent symptoms even after bypass surgery, angioplasty, stenting and available pharmacotherapy
CLI patients are at high risk of amputation and increased risk of death
Multi-billion dollar global commercial opportunity
Indication: critical limb ischemia (CLI)
17
![Page 18: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/18.jpg)
CLI: higher mortality rate than most cancers
Mustapha, J. A., Katzen, B. T., et al. (2019, May). Endovascular Today, 18(5), 80-82 18
0 100000 200000 3000000
10
20
30
40
50
60
70
80
90
No. Incident Cases in U.S.
Death within 5 years (%)
CLI
![Page 19: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/19.jpg)
CLBS12 targets patients with R4 or R5 disease
1 Reinecke H., European Heart Journal, 2015 Apr 14;36(15):932-8
CLBS12 targets patients based on the Rutherford Scale
19
CLI amputation rates increase with increasing Rutherford score (disease severity)1
Rutherford (“R”) scale
R 6: Functional foot no longer salvageable
R 5: Minor tissue loss non-healing ulcer; focal gangrene with diffuse pedal ischemia
R 4: Debilitating rest pain
R 1-3: Mild to severe claudication
![Page 20: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/20.jpg)
Post-treatment (week 12) Pre-treatment
Actual CLI Patient Laser Doppler Image
~80% of patients achieved sustainable remission within 6 months of a single treatment; durable for at least 4 years
40%
60%
70%
80%85% 85%
90%82%
0 4 8 12 24 52 104 156 208
% of Patients (CLI + BD) Achieving CLI-free Status
Time (weeks)
Kinoshita et al, Atherosclerosis 224 (2012) 440-445
Single treatment of CD34+ cells reversed CLI
20
![Page 21: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/21.jpg)
Probability of amputation-free (n=28)
0 14 28 42 57 71
Time (weeks)
CLBS12
Placebo
75%
22%
p = 0.014
Losordo, D.W. et al, Circulation 2012; 5(6):821-830
106 cells/kg
Single treatment of CD34+ cells increased amputation-free survival
21
![Page 22: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/22.jpg)
Primary Endpoint Continuous CLI-free (2 consecutive monthly visits, adjudicated independently)
Study Size 30 subjects with no-option CLI + 7 Buerger’s Disease pts.; all R4 or R5; 12 centers in Japan
Dose 106 cells/kg (CLBS12) per affected limb (studied in previous trial)
Control/Comparator Standard of Care: wound care plus drugs approved in Japan
• Including antimicrobials, antiplatelets, anticoagulants and vasodilators
Mode of administration Intramuscular, 20 injections in affected lower limb in a single treatment
Timing/Costs
Enrollment completion/results targeted for end of 2020/end of 2021,
respectively*
Earliest possible commercialization mid-2022*
Study funded to completion in current budget projections
CLBS12 registration-eligible study (Japan)
22* Timing subject to COVID-19 pandemic influence
![Page 23: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/23.jpg)
Pre 1 30 60 90 120 150 180 210 240 270 300 330 365(end)
Current Patient CLI Status (cohort completed; clinical primary endpoint met)
Natural evolution of Buerger’s Disease is continual deterioration for all patients
Surgery is not viable and existing pharmacotherapies do not prevent amputation1
CLBS12 treatment resulted in 57% of patients achieving a positive outcome
CLI-free Continuous CLI-freeRutherford 6Rutherford 4 or 5
1 Cacione DG, et al, Pharm. treatment of Buerger’s Disease, Cochrane Database of Systematic Reviews, 2016, (3) CD011033
Extraordinary CLBS12 results in Buerger’s Disease (Japan)
23
Amputation
![Page 24: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/24.jpg)
CLBS16Coronary Microvascular
Dysfunction(USA)
![Page 25: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/25.jpg)
Heart disease: still a major unmet medical need globally
1 Centers for Disease Control and Prevention as cited in McKay, Betsy. "Heart-Failure Deaths Rise, Contributing to Worsening Life Expectancy." The Wall Street Journal, 30 Oct. 2019, Link to article.2 Kochanek, KD., et al. (2016). Deaths: final data for 2014. National vital statistics reports: from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System, 65(4), 1-122. 3 ISCHEMIA Study Results, AHA Scientific Sessions November 2019. https://ischemiatrial.org/ischemia-study-results#slides
25
0 100 200 300 400 500 600 700
Suicide
Kidney failure
Influenza and Pneumonia
Diabetes
Alzheimer's
Stroke
Lower Respiratory disease
Accidents
All Cancers
Heart Disease
2017 2011
Heart Disease
Number of Deaths (thousands)1
As of 2014, 1 in 32 female deaths was from breast
cancer, but 1 in 3 was from cardiovascular disease.2
ISCHEMIA Trial3 results validate the need for treatments that go beyond large vessel
interventions
The International Study of Comparative Health Effectiveness with Medical and Invasive Approaches (ISCHEMIA) was funded by the National Heart, Lung, and Blood Institute
The study enrolled 5,179 patients at 320 sites in 37 countries
Conclusion:Interventional heart procedures do not reduce the overall rate of heart attack
or death compared with medicines and lifestyle changes alone.
![Page 26: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/26.jpg)
Deficient heart microvasculature without obstructive vessel disease
Causes frequent, debilitating chest pain that is not treatable by stents or bypass; responds poorly or not at all to available medications
Afflicts women more frequently, especially younger women1,2
Results in poor prognosis for patients with the condition3
Significantly elevated risk of all-cause mortality in women4
Quantitatively diagnosed using Coronary Flow Reserve (CFR)
CFR is the ratio of maximal to resting coronary blood flow5
Multi-billion dollar global commercial opportunity
1 Coronary Microvascular Disease. (2015, July 31). In American Heart Association2 R. David Anderson, John W. Petersen, Puja K. Mehta, et al., Journal of Interventional Cardiology, 2019: 83 Loffler and Bourque, Curr Cardiol Rep. 2016 Jan; 18(1): 1
4 Kenkre, T.S. et al., Circ: CV Qual & Outcomes 2017, 10(12) 1-95 Collins, P., British heart journal (1993) 69(4), 279–281
Indication: coronary microvascular dysfunction (CMD)
26
![Page 27: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/27.jpg)
Endpoints Therapeutic effect and the evaluation of adverse events; including changes
from baseline to 6 months for coronary flow reserve, angina frequency, CCS angina class, quality of life
Study Size 20 subjects (U.S. centers - Cedars Sinai, Los Angeles & Mayo Clinic, Rochester)
Dose Up to 300 x 106 CD34+ cells
Mode of administration Single intracoronary infusion
Timing/Cost Positive complete results presented at SCAI Scientific Sessions (May 2020)
ESCaPE-CMD: CLBS16 interventional, proof-of-concept trial
27
![Page 28: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/28.jpg)
Coronary Flow Reserve 2
CLBS16 ESCaPE-CMD results are unique and compelling
281 Murthy et al, Circulation, 20142 Henry, D. T., SCAI 2020 Scientific Sessions
CFR≤2.5 indicates CMD
CFR of 2 equates to a 3-4 fold increase of MACE at 3 years1
CFR≥2.5 is in “normal” range
Results after a single intracoronary administration of CLBS16
Pre-Treatment After 6 months
2.08
2.68p = 0.0045
N=20 N=19
![Page 29: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/29.jpg)
29
CLBS16 ESCaPE-CMD results are unique and compelling
1Spertus, J.A. et al, JACC Vol. 25, No. 2 February 1995: 333-3412 Henry, D. T., SCAI 2020 Scientific Sessions
Higher scores indicate improvement1
0 20 40 60 80 100
Treatment Satisfaction
Disease Perception
Physical Limitation
Angina Stability
Angina Frequency
Seattle Angina Questionnaire Score2
Baseline 6 months
p = 0.0117
p = 0.0026
p = 0.0247
p = 0.0156
p = 0.0005
![Page 30: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/30.jpg)
301Henry, D. T., SCAI 2020 Scientific Sessions
4.42
2.02
N=20 N=19
Pre-Treatment After 6 months
p = 0.0036
CLBS16 ESCaPE-CMD results are unique and compellingDaily Angina Frequency Decreased after 6 months1
![Page 31: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/31.jpg)
CLBS16 program status summary
31
Statistically significant improvement in heart function and symptoms
First therapy to show the ability to durably increase CFR and potentially reverse CMD after a single administration
No evidence of cell related adverse events
Expected to lead to a decreased risk of adverse cardiovascular outcomes, including CV-related death, associated with CMD
Supports microvascular repair mechanism of CD34+ cells across all indications
Represents a potential breakthrough for the treatment of CMD, a condition that affects millions in the U.S. and that disproportionately afflicts women
Next step in development (Phase 2b trial) targeted to initiate in 4Q 2020
![Page 32: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/32.jpg)
CLBS14No-Option Refractory
Disabling Angina(USA)
Regenerative Medicine Advanced Therapy (RMAT) designated - USA
![Page 33: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/33.jpg)
Recurring angina results from chronically impaired cardiac blood supply
The condition persists even after bypass surgery, angioplasty, stenting and available pharmacotherapy; no current treatment options
NORDA patients experience very frequent disabling chest pain at rest or with minimal activity
Cardiac microcirculation deficiency is the remaining treatment target
Multi-billion dollar global commercial opportunity
Indication: no-option refractory disabling angina (NORDA)
33
![Page 34: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/34.jpg)
Clinical data from double-blind, randomized, placebo-controlled clinical trials, including big pharma sponsored Phase 2 and partial Phase 31-5
Published results demonstrate:
Statistically significant improvement in exercise capacity
Statistically significant reduction in angina
Statistically significant reduction in mortality
Pristine cell safety profile
1 Losordo, D.W., et al, Circulation 2007, 115(25): 3165-72.2 Losordo, D.W., et al, Circ Res 2011, 109(4): 428-363 Povsic, T.J., et al, JACC Cardiovasc Interv, 2016 9(15): 1576-85
Our solution: CLBS14
4 Povsic, T. J. et al, European Heart Journal, 2018 39(23), 2208-22165 Velagapudi P, et al, Cardiovas Revasc Med, 2018, 20(3):215-219
34
![Page 35: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/35.jpg)
*Change in exercise time from baseline at 6 months will be the Phase 3 primary endpoint
Change in Exercise Time from Baseline (Phase 2, n=168)
58
69
140
139CLBS14 (105 cells/kg)
CLBS14 (105 cells/kg)
Placebo
Placebo
*6 months:
12 months:
p=0.014
p=0.017
sec
sec
sec
sec
CLBS14 single treatment significantly improved exercise time
35
![Page 36: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/36.jpg)
CLBS14 (105 cells/kg)
Placebo
CLBS14 (105 cells/kg)
Placebo
13.8
8.8
8.7
15.3
p=0.0421
p=0.0109
6 months:
12 months:
Reduction in Weekly Angina Frequency from Baseline (Phase 2, n=168)
CLBS14 single treatment significantly reduced angina frequency
36
![Page 37: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/37.jpg)
0 2412
10%
p = 0.0065
Time (months)
Mortality (Phase 2, n=168)
(105 cells/kg)
CLBS14
Placebo
2.5%
CLBS14 single treatment significantly improved survival
37
![Page 38: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/38.jpg)
Primary Endpoint Change in exercise time from baseline at month 6 (studied in Phase 2)
Timing 39 months from first-patient-in to top-line data; interim analysis after 50% of patients complete 6-month follow-up
Study Size ~400 subjects (~200 active, ~150 placebo, ~50 SOC with cross-over to open label treatment at 6 months)
Dose 105 cells/kg body weight (studied in Phase 2)
Control/Comparator Placebo control (blinded)
Standard-of-care (unblinded)
Mode of administration Intramyocardial injection guided by mapping catheter (NOGA)
Timing/Costs External costs: ~$70 million over a 3-4 years period Target initiation: Upon acquisition of sufficient capital that provides
confidence that the study could be funded through completion
CLBS14 Phase 3 confirmatory registration study (U.S.)
38
![Page 39: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/39.jpg)
Program 2020 2021Caladrius timeline of key development milestones*
39
CLBS119
FDA authorized IND for CLBS119 study
(COVID-19 lung damage)
Initiation of Pilot Trial Target –3Q 2020
*Timing subject to COVID-19 pandemic influence
CLBS14(NORDA)
Confirmatory Phase 3 Initiation Target: TBD (pending funding)
CLBS12(CLI)
Target Enrollment Completion by End of 2020
Top-line Data Target –End 2021/Early 2022
J-NDA Rolling Submission Initiation Target –
2H 2020
CLBS16(CMD)
Present Full ESCaPE-CMD Data – 2Q 2020
Initiation of Phase 2b Trial Target – 4Q 2020
![Page 40: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/40.jpg)
Caladrius key financial information
40
Cash & Investments:As of July 31, 20201 ~$42.0 million
Six Months Ended June 30, 2020 Operating Cash Burn:2 $10.6 millionCash Runway Based on Current Plan: End of 2021Debt as of July 31, 2020: $0
Common Shares Outstanding:As of July 31, 20203 19.3 million shares
Options Outstanding as of July 31, 2020:Exercise Price: $1.80 - $3.50 = 250,000 sharesExercise Price: > $3.50 = 911,000 shares
1.2 million shares
Warrants Outstanding as of July 31, 20204 :Weighted Average Exercise Price: $2.18 2.6 million shares
1 Includes $2.0 million in proceeds from July 2020 Private Placement, and $6.9 million in net proceeds from July 2020 ATM facility issuances2 Excludes $10.9 million in net proceeds from sale of New Jersey NOLs3 Includes ~970,000 shares from July 2020 Private Placement, and ~2.8 million shares from July 2020 ATM facility issuances4 Includes ~480,000 warrants issued from July 2020 Private Placement
![Page 41: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/41.jpg)
CD34+ cell therapy company with an advanced clinical pipeline with 2 programs with “breakthrough” designation and 1 targeting COVID-19 induced lung repair
Proprietary field-leading technology in multi-billion dollar global indications backed by a strong IP portfolio
Multiple potential value creating events in the next 12-18 months based on milestones across the pipeline (timing subject to COVID-19 pandemic influence)
Seasoned management team with noteworthy domain expertise along withbig pharma and emerging biotech experience
Strong balance sheet; ~$42 million in cash & cash equivalents (July 31, 2020) with no debt and cash runway projected to fund operations through 2021
Caladrius investment rationale
41
![Page 42: Developing Regenerative Therapies that Reverse Chronic Disease · 8/13/2020 · Possess pre-programmed tissue repair effects mediated by pro-angiogenic and anti-inflammatory functions](https://reader036.vdocuments.site/reader036/viewer/2022071001/5fbd96d23248af2aaa594b80/html5/thumbnails/42.jpg)
August 13, 2020 | Nasdaq: CLBS
Investor Re lat ions Contact:John D. Menditto
Tel : (908) [email protected]
Thank you!