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CHIMERIC THERAPEUTICS LIMITED AGM Information 2022

Nov 14, 2022

64648_rns_2022-11-14_c72652cd-06b9-4b19-b6e2-ddbb9a4fbb28.pdf

AGM Information

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Annual General Meeting Jennifer Chow CEO and Managing Director November 15, 2022

DISCLAIMER

Certain statements contained in this presentation, including, without limitation, statements containing the words “believes,” “plans,” “expects,” “anticipates,” and words of similar import, constitute “forward-looking statements.” Such forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause the actual results, performance or achievements of Chimeric (collectively, “Chimeric” or the “Company”) to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Such factors include, among others, the following: the risk that our clinical trials will be delayed and not completed on a timely basis; the risk that the results from the clinical trials are not as favorable as we anticipate; the risk that our clinical trials will be more costly than anticipated; and the risk that applicable regulatory authorities may ask for additional data,

information or studies to be completed or provided prior to their approval of our products.

Given these uncertainties, undue reliance should not be placed on such forward-looking statements. The Company disclaims any obligation to update any such factors or to publicly announce the results of any revisions to any of the forward-looking statements contained herein to reflect future events or developments except as required by law.

This presentation may not contain all the details and information necessary for you to make a decision or evaluation. Neither this presentation nor any of its contents may be used for any other purpose without the prior written consent of the Company.

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COMMITTED TO BRINGING THE PROMISE OF CELL THERAPY TO LIFE

Traditional drug development focuses on delaying disease progression - not on a cure.

We believe that novel cellular therapies have the promise to cure cancer.

To bring that promise to life for more patients, the mission of Chimeric is to discover, develop and commercialize the most promising and innovative cell therapies.

3

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“We can now conclude that CAR-T cells can CURE patients with leukemia”

Dr Carl June, MD

Richard W. Vague Professor in Immunotherapy Director of the Center for Cellular Immunotherapies at the Perelman School of Medicine

5

CELL THERAPY ANTICIPATED TO BE THE FASTEST GROWING MARKET IN ONCOLOGY

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2022 2027
MARKET MARKET
$265 BN $581BN
ONCOLOGY ONCOLOGY
$10.69 BN $42.37BN
CELL THERAPY CELL THERAPY
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CAGR
8.2%
ONCOLOGY
31.7%
CELL THERAPY
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Market Data Forecast, Global Cell Therapy Market Size, Share, Trends, Growth & COVID-19 Impact Analysis Report – Segmented By Technology, Type, Cell Source, Application, End-Users and Region (North America, Europe, Asia-Pacific, Latin America, Middle East and Africa) – Industry Forecast (2022 to 2027)

CHIMERIC THERAPEUTICS CORPORATE SNAPSHOT

  • Multiple Assets with Positive Phase 1 Signals

  • Robust Clinical Development Plans with Broad Therapeutic Focus

  • Innovative and Diversified Portfolio of Next Generation Technologies

  • Industry Leading Team with Extensive Cell Therapy Experience

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ASX: CHM
0.31
0.16
0.14
0.12
0.08
Nov. 21 Feb. 22 May 22 Aug. 22 Nov. 22
Share Price Nov. 13: Market Cap Nov. 13: ~$36M
52 Week Range: 0.08-0.31 Net Cash: AUS $8M (Sept 22)
Shares on Issue: 425 M Board / Mgmt. Ownership: 20%
Share Price AUS ($)
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A YEAR OF MAJOR MILESTONES: November 2021- November 2022

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CORE NK Option CDH17 CAR T CORE NK CDH17 VECTOR CORE NK
(CHM 0201) (CHM 2101) (CHM 0201) (CHM 2101) (CHM 0201)
From Case Western Sponsored Research Exercise of Licensed from University Sponsored Research
Reserve University Agreement with Penn Option of Pennsylvania Agreement
November February November
May June
2021 2022 2022 2022 2022
November February March
March June
2021 2022 2022
2022 2022
Positive DL1 Data Positive DL2 Data CDH17
Positive Phase 1 Data CORE NK
Phase 1A CLTX CAR T Phase 1A CLTX CAR T Nature Cancer
CORE NK Combination Trial
(CHM 1101) (CHM 1101) Preclinical
Clinical Trial Clinical Trial (CHM 0201) Clearance from FDA
Publication Clinical Trial
(CHM 0201+)
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CHIMERIC CELL THERAPY PORTFOLIO

CUTTING EDGE INNOVATION WITH BROAD COMMERCIAL OPPORTUNITY

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Novel Design
T Cells NK Cells
Autologous Allogeneic
(personal) (off-the-shelf)
CORE-NK Platform
Phase 1 Complete
CLTX CAR T CLTX CAR T
CDH17 CAR T
(ICT/ ICV) (IV) Next Gen. CLTX CDH17 Undisclosed
CORE-NK
GBM Solid CAR-NK CAR-NK CAR-NK
Platform
Solid Tumor
Phase 1 Tumor
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DIFFERENTIATING CHIMERIC A DIVERSIFIED PORTFOLIO WITH A FOCUS ON CURATIVE INTENT

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Cancer Target Innovation T Cell Derived Therapies NK Cell Derived Therapies Personalized (Autologous) Therapies Off the Shelf (Allogeneic) Therapies

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CHIMERIC MANAGEMENT TEAM EXPERTS IN CELL THERAPY DEVELOPMENT & COMMERCIALIZATION

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EXPERIENCE EXPERTISE
Years of Cell
75+ Therapy Experience 50+ Development Programs
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PROVEN Of the FDA-Approved 4/6 CAR T Cell Therapies

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Dr Jason
LITTEN
Chief Medical
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Dr Li
REN
Vice President
Technical
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Dr Eliot
BOURK
Chief Business
Officer
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Dr Stephanie
ASTROW
Vice President
Translational
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Cassandra
HARRISON
Vice President
Clinical Operations
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CHM 0201, 0301, 1301, 2301, 3301 Natural Killer Cell Therapies

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OFF THE SHELF (ALLOGENEIC) NK THERAPY DEVELOPMENT ON DEMAND THERAPY

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Leukapheresis (blood draw) from a healthy donor

Healthier starting material

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Isolation of the Natural Killer Cells

Engineering of the Natural Killer Cells

1000’s of Doses Manufactured at Once

Scalable Rapidly manufacturing available, with reduced off the costs shelf

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Off the Shelf Availability for Patients on Demand

Ability to reach more patients

CHM 0201 PHASE 1 STUDY RESULTS PROMISING RESULTS ACROSS ALL KEY ENDPOINTS

PERSISTENCE

SAFETY

ESTABLISHED SAFETY 28 DAY across 3 Dose PERSISTENCE OF Levels CORE NK CELLS NO GVHD WITH DEMONSTRATED UNIVERSAL DONOR CELLS

EXPANSION

LARGE SCALE MANUFACTURING SUCCESS FROM A SINGLE DONOR

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EFFICACY IN EFFICACY IN SOLID BLOOD TUMOURS CANCERS 33% DISEASE 100% DISEASE CONTROL RATE CONTROL RATE IN SOLID IN BLOOD TUMOURS CANCERS 66% DURABILITY 15+ MONTH OF RESPONSE COMPLETE PAST DAY 100 RESPONSE

Transplantation and Cellular Therapy, 2022, ISSN 2666-6367

CORE NK (CHM 0201) PHASE 1 STUDY RESULTS ONGOING COMPLETE RESPONSE

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PATIENT #8
33-year-old female
DIAGNOSIS : AML with therapy
related High-Risk MDS with
circulating blasts and high tumour
burden
HISTORY: Progressive disease
with prior allogeneic transplant
SAFETY: N o dose limiting
toxicities, no cytokine release
syndrome, no GvHD
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COMPLETE
CORE NK
RESPONSE
INFUSION
DAY 0, 14 DAY 100
CORE NK cell treatment at Enabling patient to
25 X 10 [6 ] cells/ kg undergo transplant
ONGOING
STABLE
COMPLETE
DISEASE
RESPONSE
DAY 28
15+ MONTHS
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Transplantation and Cellular Therapy, 2022, ISSN 2666-6367

ENHANCING THE CHM 0201 EFFICACY SIGNAL NEW PHASE 1B CHM 0201 CLINICAL TRIAL

To identify a combination therapy that could enhance the initial efficacy signal seen with CHM 0201 (CORE NK) cells by modulating the tumour microenvironment CHM 0201 + VACTOSERTIB

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CORE (Clinically validated, off the shelf, robust and enhanced) NK cells

A clinical drug candidate that inhibits TGF- β signaling, modulating the tumour microenvironment

FDA APPROVED FIRST EVER TRIAL OF NK CELLS WITH VACTOSERTIB

A Phase Ib Study to Evaluate Safety and Persistence of ex Vivo Expanded Universal Donor NK Cells in Combination With IL-2 and TGFbeta Receptor I Inhibitor Vactosertib

Study Initiation: Sept. 9, 2022 Enrollment: 12 Patients Estimated Completion: Dec. 2023

Eligible Patients: Relapse or refractory solid tumours and hematological malignancies

Clinical Trials.gov Identifier: NCT05400122

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CHM 1101 CLTX CAR T Cell Therapy

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PERSONALIZED (AUTOLOGOUS) T CELL THERAPY DEVELOPMENT HARNESSING AN INDIVIDUAL’S OWN IMMUNE SYSTEM

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John
John
Leukapheresis (blood draw) Isolation of the Engineering of the Individual patients Personalized therapy for
from an individual patient T Cells T Cells with Chimeric engineered CAR T Cells the individual patient
Antigen Receptors (CARs) are frozen for transport
Starting cells Unlikely that a patient’s No need for Proven to be
curative in blood
come from own immune system will anti-rejection
individual patient attack the cells medications cancers
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CHM 1101 (CLTX CAR T) Encouraging Initial Data in Glioblastoma

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Post-CLTX CAR T
7 infusions
Nov 4, 2020 No recurrence
of CHM 1101
treated
tumour
Rapid tumour
progression
where CHM
1101 was not
administered
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“This preliminary data is encouraging as it demonstrates safety with dual routes of administration. We now look forward to advancing the trial to higher dose levels which may provide more therapeutic benefit to patients”

Behnam Badie, M.D., Professor and Chief, Division of Neurosurgery; Director, Brain Tumor Program, Department of Surgery, City of Hope.

SNO 2021, Abstract CTIM-29, “Clinical evaluation of chlorotoxin-directed CAR T cells for patients with recurrent glioblastoma”

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CHM 2101 CDH17 CAR T Cell Therapy

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CHM 2101: (CDH17 CAR T) A NOVEL 3rd GENERATION CAR T DESIGNED FOR SOLID TUMORS AND HEADED TO THE CLINIC

Preclinical data featured in Nature Cancer

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Efficacy
Complete eradication of tumor
cells with no relapse
18
Dr. Xianxin Hua, 00
M.D., Ph.D.
12
00
60
0
0
Days after CAR T Cell
Injection
Dr. Carl June
M.D.
)
3
Tumor volume (mm
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Safety

High tumor-specific activity in vivo with no on-target / off-tumor toxicity

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Feng et al. Nature Cancer, 2022. https://doi.org/10.1038/s43018-022-00344-7

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AUSTRALIA’S MOST ROBUST AND ADVANCED CELL THERAPY PORTFOLIO AND PIPELINE

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NOV. 2022
JAN. 2021
1 7
ASSETS IN
ASSET IN
DEVELOPMENT
DEVELOPMENT
3
1
ONGOING CLINICAL ONGOING CLINICAL
TRIAL TRIALS
2
0
TRIALS WITH EARLY TRIALS WITH EARLY
POSITIVE CLINICAL POSITIVE CLINICAL
SIGNALS SIGNALS
1 10
DISEASE AREA IN DISEASE AREAS IN
DEVELOPMENT DEVELOPMENT
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NEXT 6-12
MONTHS
KEY
MILESTONES
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CHM 2101 FDA IND Clearance CHM 2101 Manufacture & Release of CDH17 Vector CHM 1101 Completion of GBM Phase 1 Dose Escalation CHM 1101 Second CHM GBM Trial Site Initiation CHM 1101 First Patient Dosed CHM GBM Trial CHM 1101 Initiation of CHM Ph. 1A/B GBM Trial CHM 0201 First Patient Dosed in CORE NK Combo Trial CHM 1101 Completion of COH Dose Level 3 CHM 0301 Execute SRA with CWRU CHM 0201 Execute CORE NK Licensing Agreement CHM 0201 FDA Clearance for CORE NK Combo Trial CHM 2101 Execute Agreement for CDH17 Vector License CHM 2101 Technology Transfer of CDH17 to WuXi CHM 1101 Manufacture & Release of CLTX Vector CHM 1101 Strategic Partnerships to Support GBM Trial

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Opportunity

Clinical Promise

Initial positive signals from 2 phase 1 clinical trials

7 novel assets in the fast-growing segment in oncology drug development

Australian Leadership in Cell Therapy

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Near Term Value Multiple key clinical milestones over the next 12 – 24 months creating value

Proven Expertise

World class team with success driving development to commercial approval

CONTACT INFORMATION

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Jennifer Chow Chief Executive Officer Chimeric Therapeutics Ltd Cell: +1 908-723-8387 [email protected]

Paul A. Hopper Executive Chairman Chimeric Therapeutics Ltd Cell: +61 406671515 [email protected]

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