Kura Oncology Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
February 07 2025 - 6:30AM
Kura Oncology, Inc. (the “Company”) (Nasdaq: KURA), a
clinical-stage biopharmaceutical company committed to realizing the
promise of precision medicines for the treatment of cancer, today
announced that on February 3, 2025, the Compensation Committee of
the Company’s Board of Directors (the “Compensation Committee”)
granted inducement awards consisting of nonstatutory stock options
to purchase 164,000 shares of common stock to nine (9) new
employees under the Company’s 2023 Inducement Option Plan, as
amended. The Compensation Committee approved the stock options as
an inducement material to such employees’ employment in accordance
with Nasdaq Listing Rule 5635(c)(4).
Each stock option has an exercise price equal to
$8.25 per share, the Company’s closing sales price on February 3,
2025, and will vest over four years, with 25% of the underlying
shares vesting on the one-year anniversary of the applicable
vesting commencement date and the balance of the underlying shares
vesting monthly thereafter over 36 months, subject to the new
employees’ continued service relationship with the Company through
the applicable vesting dates. The stock options are subject to the
terms and conditions of the Company’s 2023 Inducement Option Plan,
as amended, and the terms and conditions of an applicable stock
option agreement covering the grant.
About Kura Oncology
Kura Oncology is a clinical-stage
biopharmaceutical company committed to realizing the promise of
precision medicines for the treatment of cancer. The Company’s
pipeline consists of small molecule drug candidates that target
cancer signaling pathways. Ziftomenib, a once-daily, oral menin
inhibitor, is the first and only investigational therapy to receive
Breakthrough Therapy Designation from the U.S. Food and Drug
Administration (the “FDA”) for the treatment of relapsed/refractory
(“R/R”) NPM1-mutant acute myeloid leukemia (“AML”). In November
2024, Kura Oncology entered a global strategic collaboration
agreement with Kyowa Kirin Co., Ltd. to develop and commercialize
ziftomenib for AML and other hematologic malignancies. Enrollment
in a Phase 2 registration-directed trial of ziftomenib in R/R
NPM1-mutant AML has been completed, and the companies anticipate
submission of a New Drug Application to the FDA in the second
quarter of 2025. Kura Oncology and Kyowa Kirin are also conducting
a series of clinical trials to evaluate ziftomenib in combination
with current standards of care in newly diagnosed and R/R
NPM1-mutant and KMT2A-rearranged AML. KO-2806, a next-generation
farnesyl transferase inhibitor, is being evaluated in a Phase 1
dose-escalation trial as a monotherapy and in combination with
targeted therapies. Tipifarnib, a potent and selective farnesyl
transferase inhibitor, is currently in a Phase 1/2 trial in
combination with alpelisib for patients with PIK3CA-dependent head
and neck squamous cell carcinoma. For additional information,
please visit Kura’s website at https://kuraoncology.com/ and follow
us on X and LinkedIn.
Contacts
Investors:Patti BankManaging Director(415)
513-1284patti.bank@icrhealthcare.com
Media:Alexandra WeingartenAssociate Director,
Corporate Communications & Investor Relations(858)
500-8822alexandra@kuraoncology.com
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