DEVELOPING PRECISION MEDICINES FOR THE TREATMENT OF CANCER

Corporate Presentation - May 2023

FORWARD-LOOKING STATEMENTS

This presentation contains forward-looking statements. Such statements include, but are not limited to, statements regarding our research, preclinical and clinical development activities, plans and projected timelines for ziftomenib, tipifarnib and KO-2806, plans regarding regulatory filings, our expectations regarding the relative benefits of our product candidates versus competitive therapies, and our expectations regarding the therapeutic and commercial potential of our product candidates. The words "believe," "may," "should," "will," "estimate," "promise," "plan", "continue," "anticipate," "intend," "expect," "potential" and similar expressions (including the negative thereof), are intended to identify forward-looking statements. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Risks that contribute to the uncertain nature of the forward-looking statements include: our preclinical studies and clinical trials may not be successful; the U.S. Food and Drug Administration (FDA) may not agree with our interpretation of the data from clinical trials of our product candidates; we may decide, or the FDA may require us, to conduct additional clinical trials or to modify our ongoing clinical trials; we may experience delays in the commencement, enrollment, completion or analysis of clinical testing for our product candidates, or significant issues regarding the adequacy of our clinical trial designs or the execution of our clinical trials may arise, which could result in increased costs and delays, or limit our ability to obtain regulatory approval; the commencement, enrollment and completion of clinical trials and the reporting of data therefrom; the COVID-19 pandemic may disrupt our business and that of the third parties on which we depend, including delaying or otherwise disrupting our clinical trials and preclinical studies, manufacturing and supply chain, or impairing employee productivity; our product candidates may not receive regulatory approval or be successfully commercialized; unexpected adverse side effects or inadequate therapeutic efficacy of our product candidates could delay or prevent regulatory approval or commercialization; and we may not be able to obtain additional financing. Additional risks and uncertainties may emerge from time to time, and it is not possible for Kura's management to predict all risk factors and uncertainties.

All forward-looking statements contained in this presentation speak only as of the date on which they were made. Other risks and uncertainties affecting us are described more fully in our filings with the Securities and Exchange Commission. We undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

This presentation also contains statistical and clinical data obtained from and prepared by third parties. The recipient is cautioned not to give undue weight to such disclosures. Neither the Company nor any other person makes any representation as to the accuracy or completeness of such data or undertakes any obligation to update such data after the date of this presentation.

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INVESTMENT HIGHLIGHTS

Targeted

Advancing a pipeline of novel therapies, forging new scientific and clinical paths to give patients a

Oncology

better chance for long-term durable remissions

Menin Inhibitor Program (ziftomenib)

Potential to address 35% or more of acute leukemias

Encouraging safety, tolerability and clinical activity observed in relapsed/refractory AML patients

30% CR rate among 20 patients with NPM1 mutations treated at RP2D

Proprietary

Enrollment ongoing in Phase 2 registration-directed trial in NPM1-mutant AML

First combination study with standards of care expected to begin in 1H 2023

Pipeline

Farnesyl Transferase Inhibitor Programs (tipifarnib & KO-2806)

  • Durable responses as a monotherapy in recurrent/metastatic HRAS-mutant HNSCC patients
  • Proof of mechanism demonstrated in combination with alpelisib in PIK3CA-dependent HNSCC
  • Preclinical data support potential to prevent emergence of resistance to targeted therapies
  • FDA clearance of IND for KO-2806,next-generation FTI; on track to initiate Phase 1 study in 2H 2023

Strong

$25 million strategic equity investment from Bristol Myers Squibb

Financials

$406 million in cash as of March 31, 2023* provides runway into Q4 2025

* Cash, cash equivalents and short-term investments

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KURA LEADERSHIP TEAM AND BOARD OF DIRECTORS

Leadership Team

Troy Wilson, Ph.D., J.D.

Teresa Bair, J.D.

Stephen Dale, M.D.

Kathy Ford

President &

Chief Legal Officer

Chief Medical Officer

Chief Operating Officer

Chief Executive Officer

Francis Burrows, Ph.D.

Pete De Spain

Tom Doyle

Mollie Leoni, M.D.

Senior Vice President,

Senior Vice President, Investor

Senior Vice President,

Senior Vice President,

Translational Research

Relations & Corporate

Finance & Accounting

Clinical Development

Communications

Board of Directors

Troy Wilson, Ph.D., J.D.

Faheem Hasnain

Helen Collins, M.D.

Thomas Malley

Chairman

Lead Independent Director

Carol Schafer

Steven Stein, M.D.

Diane Parks

Mary Szela

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DRUG CANDIDATE PIPELINE

PROGRAM

CLINICAL TRIAL

PLANNED

STUDY STARTUP

PHASE 1

REGISTRATION DIRECTED

KOMET-001

NPM1-mutant acute myeloid leukemia (AML)

Monotherapy

Non-NPM1-m /Non-KMT2A-r AML

(Relapsed/

refractory)

KMT2A-rearranged ALL

KOMET-007

ZIFTOMENIB

Combinations

NPM1-mutant AML

Menin Inhibitor

with ven/aza, 7+3

(Relapsed/

KMT2A-rearranged AML

refractory,

frontline)

KOMET-008

Combinations

NPM1-mutant AML

with gilteritinib,

FLAG-IDA, LDAC

KMT2A-rearranged AML

(Relapsed/

refractory)

TIPIFARNIB

KURRENT-HN

Farnesyl

Combination with PIK3CA-dependent HNSCC

Transferase

alpelisib

Inhibitor (FTI)

KO-2806

FIT-001

Clear Cell Renal Cell Carcinoma

Next-Generation

Combinations

Non-Small Cell Lung Cancer

with targeted

FTI

therapies

Other Solid Tumors

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Disclaimer

Kura Oncology Inc. published this content on 10 May 2023 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 10 May 2023 20:32:18 UTC.