Company profile / KURA

Kura Oncology

Clinaptis stanceConstructive
ConvictionLow
Ticker
KURA
Exchange
NASDAQ
Coverage
Standard profile
Updated
Sep 12, 2026
Precision Oncology / Hematology

Commercial-stage precision-oncology company led by KOMZIFTI (ziftomenib), a once-daily menin inhibitor approved for adults with relapsed or refractory NPM1-mutated acute myeloid leukemia. Development now centers on frontline AML combinations, with the next-generation farnesyl-transferase inhibitor darlifarnib providing earlier solid-tumor optionality.

01 / Clinaptis view

The current read

Initial read: commercially encouraging, but the discount is less obvious than the cash balance makes it look. At the September 11 close, Kura's headline enterprise value was approximately $0.50 billion.

  1. That is about 6x annualized 2Q26 reported revenue—not 1.7x—and even that multiple is a poor shorthand because collaboration revenue is not recurring product economics. The launch is real: KOMZIFTI produced $9.1 million in 2Q26 revenue, approximately 115 new starts and more than 250 total prescriptions.
  2. Kura says it won a majority of new R/R NPM1-mutated AML starts within the menin class. Once-daily dosing and the absence of Revuforj's boxed QTc/Torsades warning are credible commercial advantages, although KOMZIFTI still requires ECG, electrolyte and drug-interaction management.
  3. The economics are shared: Kura retains 50% of U.S. profit, funds the agreed global development plan through 2028 and currently addresses adults with R/R NPM1-mutated AML only. Syndax retains broader KMT2A and pediatric labels, so the valuation gap is not just a market-share judgment.
  4. The value step-up is also deferred. KOMET-007 produced 96% and 90% CRc rates in newly diagnosed NPM1-mutated and KMT2A-rearranged AML, respectively, with 94% 12-month survival in NPM1.
  5. Those results are impressive, but uncontrolled and layered onto active chemotherapy. The approximately 1,300-patient KOMET-017 program is the test; first pivotal topline is guided to 2028.
  6. Darlifarnib is legitimate optionality, not current value support. Its randomized cabozantinib comparison in clear-cell RCC is the first cleaner contribution test and is due in 2H27.
  7. The old tipifarnib/HNSCC thesis should stay out of base value unless Kura commits to a new darlifarnib combination program.
02 / Consensus gap

Where the market may differ

The bullish read is that the market is overlooking an approved drug winning early new-start share, a balance sheet that reaches the pivotal readout and unusually strong frontline response data. If repeat prescriptions show Revuforj-like persistence, the launch can compound faster than current revenue suggests.

  1. The harder read is that Kura is winning flow while Syndax owns the installed base—and in AML, duration monetizes the installed base. A new-start lead does not close the revenue gap unless KOMZIFTI patients remain on treatment and generate repeats.
  2. The next quarterly update therefore matters more for repeat prescriptions and revenue per start than for another share headline. There is also a two-year evidence gap.
  3. The 2H26 datasets can strengthen the combination narrative, but none is randomized. KURA offers greater percentage sensitivity to a successful frontline program; the 50/50 U.S. split, narrower current label and 2028 timing explain why that upside is not free.
Coverage state
Standard profile
What the review turns on
Key variable

Whether early NPM1 new-start share converts into durable prescriptions—and whether KOMET-017 proves that ziftomenib adds frontline benefit to already-active AML backbones

Next catalyst

KOMZIFTI · 3Q26 revenue and repeat-prescription update · Next quarterly results; Ziftomenib combinations · frontline and FLT3-mutated AML data · 2H 2026

03 / Pipeline

Key programs

5 assets · 6 programs

AssetIndicationStageNext event
KOMZIFTI (ziftomenib)
R/R NPM1-mutated AML in adults
FDA approved / commercial
3Q26 revenue, new starts and repeat prescriptions; watch whether early new-start share converts into treatment duration
Ziftomenib · KOMET-017
Newly diagnosed NPM1-mutated and KMT2A-rearranged AML
Phase 3
Two randomized frontline studies totaling approximately 1,300 planned patients; first pivotal topline guided to 2028
Ziftomenib · KOMET-007 / KOMET-008
Frontline and R/R AML combinations, including FLT3-mutated disease
Phase 1 / 2
Updated venetoclax/azacitidine durability plus initial 7+3/quizartinib and gilteritinib combinations in 2H 2026
Darlifarnib
Clear-cell renal-cell carcinoma
Randomized Phase 1b
Initial darlifarnib/cabozantinib versus cabozantinib data expected in 2H 2027
KRAS-mutated solid tumors
Phase 1 / platform development
Darlifarnib/daraxonrasib arm in second-line-or-later pancreatic cancer planned to begin in 1H 2027
Ziftomenib · KOMET-015
Advanced gastrointestinal stromal tumors after imatinib failure
Phase 1
Early proof-of-concept evaluation with imatinib; no efficacy readout timing disclosed
04 / Connected research

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