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Kura Oncology and Kyowa Kirin Announce Presentations of Ziftomenib Ven/Aza Combination Data in Frontline and Relapsed/Refractory NPM1-m or KMT2A-r Acute Myeloid Leukemia at 2025 ASH Annual Meeting

Key Takeaway: Kura Oncology and Kyowa Kirin will present data from the KOMET-007 trial at the ASH 2025 Annual Meeting. The trial evaluates ziftomenib in combination with standard therapies for acute myeloid leukemia (AML). The presentations will include updated safety and clinical activity results for both newly diagnosed and relapsed/refractory AML patients. This research aims to enhance treatment options for AML patients.
Price reaction · baseline $10.27 (2025-10-31 close) · hit pre-market · 2 other KURA headline(s) in the window, move may be shared
day 0 close · peak
-4.9%

Market Sentiment Analysis

POSITIVE FACTORS

  • Ziftomenib shows promise in treating AML with venetoclax and azacitidine.
  • Data from the KOMET-007 trial will be presented at a major conference.
  • The study aims to benefit a large number of patients with AML.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+116%
120-day peak, hindsight
Typical move
5.7%
average across 9 past catalysts
Cash runway
~25 mo
Low dilution risk
Lead asset
Tipifarnib
Phase 2 · Leukemia, Myelomonocytic, Chronic

Full Press Release Details

– Data to be featured in two oral presentations on December 8, 2025 –
– Broad development program assesses ziftomenib across diverse AML segments and treatment paradigms to inform appropriate use –
SAN DIEGO and TOKYO, Nov. 03, 2025 (GLOBE NEWSWIRE) -- Kura Oncology, Inc. (Nasdaq: KURA, “Kura”) and Kyowa Kirin Co., Ltd. (TSE: 4151, “Kyowa Kirin”) today announced that results from the KOMET-007 combination trial of ziftomenib, a once-daily, oral investigational menin inhibitor, will be featured in two oral presentations at the upcoming American Society of Hematology (ASH) 2025 Annual Meeting, on December 8, 2025 in Orlando, FL.
KOMET-007 is an ongoing Phase 1a/b dose-escalation/expansion study of ziftomenib in combination with standard-of-care chemotherapies in adults withNPM1-mutated (NPM1-m) orKMT2A-rearranged (KMT2A-r) acute myeloid leukemia (AML). The combination data presented at ASH will include data in both newly diagnosed adults withNPM1-m AML and updated data in adults with relapsed or refractoryNPM1-m orKMT2A-r AML treated with ziftomenib in combination with the non-intensive chemotherapy regimen of venetoclax and azacitidine (ven/aza).
The two ziftomenib abstracts are based on an earlier data cutoff of June 2025, in line with ASH submission timelines. The oral presentations at ASH will include more mature data, including additional response-evaluable patients, longer follow-up and expanded safety summaries.
“At ASH 2025, we look forward to sharing data evaluating ziftomenib with venetoclax / azacitidine in both the newly diagnosed and relapsed/refractory AML settings,” said Mollie Leoni, M.D., Chief Medical Officer of Kura Oncology. “These trials are part of a comprehensive and focused clinical development plan designed to understand how menin inhibition can benefit the greatest number of patients in need. We expect to continue generating data from the combination of ziftomenib with commonly used treatment backbones across multiple trials, including the KOMET-017 Phase 3 trial. The emerging profile from this effort gives us confidence that ziftomenib as monotherapy and in combination represents a meaningful step forward for patients if these findings are confirmed.”

ASH Presentations:

Ziftomenib in Combination with Venetoclax and Azacitidine in Relapsed / RefractoryNPM1-m orKMT2A-r Acute Myeloid Leukemia: Updated Phase 1a/b safety and clinical activity results from KOMET-007Session 616. Menin inhibitors and FLT3 inhibitors in AMLMonday, December 8, 2025; 10:45-11:00 AM ETChapin Theater (320)Oral #764
Ziftomenib in Combination with Venetoclax and Azacitidine in Newly DiagnosedNPM1-m Acute Myeloid Leukemia: Phase 1b Results from KOMET-007Session 616. Menin inhibitors and FLT3 inhibitors in AMLMonday, December 8, 2025; 11:15-11:30 AM ETChapin Theater (320)Oral #766
Copies of the presentations will be available on Kura's website atwww.kuraoncology.com/pipeline/publications/following presentation at the meeting.
About Kura OncologyKura Oncology is a clinical-stage biopharmaceutical company committed to realizing the promise of precision medicines for the treatment of cancer. The Company’s pipeline of small molecule drug candidates is designed to target cancer signaling pathways and address high-need hematologic malignancies and solid tumors. Kura is developing ziftomenib, a menin inhibitor targeting certain genetic drivers of acute myeloid leukemias, and continues to pioneer advancements in menin inhibition for acute leukemias and solid tumors and in farnesyl transferase inhibition to address mechanisms of adaptive and innate resistance in the treatment of solid tumors. For additional information, please visit the Kura website athttps://kuraoncology.com/and follow us onXandLinkedIn.
About Kyowa KirinKyowa Kirin aims to discover and deliver novel medicines and treatments with life-changing value. As a Japan-based Global Specialty Pharmaceutical Company, Kyowa Kirin has invested in drug discovery and biotechnology innovation for more than 70 years and is currently working to engineer the next generation of antibodies and cell and gene therapies with the potential to help patients with high unmet medical needs, such as bone & mineral, intractable hematological diseases/hemato-oncology and rare diseases. A shared commitment to Kyowa Kirin’s values, to sustainable growth, and to making people smile unites Kyowa Kirin across the globe. You can learn more about the business of Kyowa Kirin atwww.kyowakirin.com.
Kura Forward-Looking StatementsThis news release contains certain forward-looking statements that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. Such forward-looking statements include statements regarding, among other things, the expected timing and presentation of results and data from the KOMET-007 clinical trial; the expectation of continued data generation from the combination of ziftomenib with commonly used treatment backbones across multiple trials, including the KOMET-017 trials; and the therapeutic potential of ziftomenib as a monotherapy and in combination with commonly used treatment backbones;. Factors that may cause actual results to differ materially include the risk that compounds that appeared promising in early clinical trials do not demonstrate safety and/or efficacy in later clinical trials; uncertainties associated with performing clinical trials, regulatory filings, and other interactions with regulatory bodies; risks associated with reliance on third parties to successfully conduct clinical trials; the risk that the collaboration with Kyowa Kirin is unsuccessful; and other risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such drugs. You are urged to consider statements that include the words “may,” “will,” “would,” “could,” “should,” “believes,” “estimates,” “projects,” “promise,” “potential,” “expects,” “plans,” “anticipates,” “intends,” “continues,” “designed,” “goal,” or the negative of those words or other comparable words to be uncertain and forward-looking. For a further list and description of the risks and uncertainties Kura faces, please refer to Kura's periodic and other filings with the Securities and Exchange Commission, which are available at www.sec.gov. Such forward-looking statements are current only as of the date they are made, and Kura assumes no obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

Kura Contact

Kyowa Kirin Contacts

Frequently Asked Questions

What is the KOMET-007 trial?

The KOMET-007 trial is a Phase 1a/b study assessing ziftomenib combined with standard therapies for AML.

When will the data from the trial be presented?

The data will be presented on December 8, 2025, at the ASH Annual Meeting.

What types of AML are being studied?

The study focuses on NPM1-mutated and KMT2A-rearranged acute myeloid leukemia.

What is the significance of ziftomenib?

Ziftomenib is a menin inhibitor that may improve treatment outcomes for AML patients.

Last updated: Nov 3, 2025