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WHWK

Whitehawk Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 2·Morristown, NJ, United States·CEO: Dr. David J. Lennon Ph.D.
Oncology

WHWK evidence brief

What we can confirm

BioSniper Score:
6.3 / 10
Market Cap:
$234.3M
Lead Asset:
fyarro (Phase 2)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $234.3M · Lead Asset: fyarro (Phase 2)
BioSniper AIPage evidence connected

Prepared research question

What matters most for WHWK—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · WHWK

Whitehawk Therapeutics, Inc. is a clinical-stage oncology company developing antibody-drug conjugates (ADCs) and has one marketed product, FYARRO (nab-sirolimus), for advanced PEComa.

Key risk: No revenue, net loss

6.3/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$234.3M

Cash Runway

—

Lead Asset

fyarro (Phase 2)

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 2 clinical trials · 1 catalyst for Whitehawk Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Whitehawk Therapeutics, Inc. is a clinical-stage oncology company developing antibody-drug conjugates (ADCs) and has one marketed product, FYARRO (nab-sirolimus), for advanced PEComa.

  • Cash & equivalents of $85.2M as of 2026-06-30 [sec].
  • Total revenue of $0.0M and net income of -$16.6M as of 2026-06-30 [sec].
  • Phase 1 trials for HWK-007 (PTK7-directed ADC) and HWK-016 (MUC16-directed ADC) are actively recruiting; data readouts expected in first half of 2027 [sec_mda · as of 2026-05-07].
  • IND for HWK-206 (biparatopic ADC targeting SEZ6) is anticipated to be cleared by the FDA in mid-2026 [sec_mda · as of 2026-08-06].
  • Entered into a global collaboration with Biocytogen in June 2026 to develop bispecific antibody-drug conjugates [sec_mda · as of 2026-08-06].

What works

  • Strong cash position of $85.2M as of 2026-06-30 provides runway for ongoing Phase 1 trials and pipeline expansion [sec].
  • Multiple ADC programs in Phase 1 (HWK-007, HWK-016) with a third (HWK-206) expected to enter the clinic soon, targeting large oncology indications [sec_mda · as of 2026-05-07].
  • Recent strategic collaborations (Hangzhou DAC option agreement, Biocytogen BsADC collaboration) expand the company's ADC pipeline without diluting global rights [sec_mda · as of 2026-08-06].
  • Management team has extensive experience in oncology drug development and commercialization [sec_mda · as of 2026-08-06].

What to weigh

  • No revenue generated as of 2026-06-30, with a net loss of $16.6M in the latest reported period [sec].
  • All pipeline candidates are in early Phase 1 trials; no clinical data have been reported yet, and data readouts are not expected until the first half of 2027 [sec_mda · as of 2026-05-07].
  • The company relies on external partners (WuXi Biologics, Hangzhou DAC, Biocytogen) for key ADC technology and manufacturing, creating dependency risks [sec_mda · as of 2026-05-07].
  • Patent expiry for FYARRO (sirolimus) is scheduled for 2040-10-28, which could eventually affect the only commercialized product's exclusivity [catalyst].

From the filings

Quoted directly from source documents.

  • Phase 1 trials for HWK-007 and HWK-016 are actively recruiting with data readouts expected in first half of 2027

    “The FDA has cleared the IND applications for HWK-007 and HWK-016 and the Phase 1 trials for each asset are now actively recruiting. We expect data readouts in the first half of 2027 for each trial.”

    SEC MD&A · May 7, 2026

  • IND for HWK-206 anticipated in mid-2026

    “We anticipate FDA clearance of our IND for HWK-206 for the treatment of small cell lung cancer ("SCLC") and neuroendocrine tumors ("NETs") in mid-2026.”

    SEC MD&A · August 6, 2026

  • Collaboration with Biocytogen for bispecific ADCs

    “in June 2026, we entered into a global collaboration with Biocytogen to develop bispecific antibody-drug conjugates ("BsADC").”

    SEC MD&A · August 6, 2026

Catalyst timeline

  • 2040-10-28 · Patent_Expiry · SIROLIMUS — Patent expiry for NDA213312 (FYARRO/sirolimus); may affect exclusivity of the company's only commercialized product.
Risks & what to watch (4)›

Key risks

  • No revenue, net loss — Zero revenue and $16.6M net loss as of 2026-06-30; company is pre-revenue and dependent on cash reserves [sec].
  • Early-stage pipeline — All candidates are in Phase 1; no clinical data available yet, with first readouts not expected until H1 2027 [sec_mda · as of 2026-05-07].
  • Partner dependency — Key ADC technology and manufacturing rely on partners (WuXi, Hangzhou DAC, Biocytogen), creating execution and IP risks [sec_mda · as of 2026-05-07].
  • Patent expiry for FYARRO — Patent for FYARRO (sirolimus) expires 2040-10-28, potentially affecting long-term product exclusivity [catalyst].

What to watch

  • FDA clearance of IND for HWK-206, expected mid-2026 [sec_mda · as of 2026-08-06].
  • Phase 1 data readouts for HWK-007 and HWK-016, expected in the first half of 2027 [sec_mda · as of 2026-05-07].
  • Submission of IND applications for new ADC programs under the Hangzhou DAC option agreement, anticipated over the next 12-24 months [sec_mda · as of 2026-08-06].
  • Progress of the Biocytogen bispecific ADC collaboration, announced in June 2026 [sec_mda · as of 2026-08-06].

Sources: Catalysts · Pipeline · SEC MD&A · Generated October 13, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.9

D/E 0.06 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth7.2

4 candidates

Catalyst Momentum2.0

1 upcoming, next in ~5128d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

62

Total value held

$122.4M

HolderSharesValue
qvt financial lp4,615,709$15.9M
orbimed advisors llc4,166,000$14.4M
suvretta capital management, llc3,700,000$12.8M
acuta capital partners, llc3,410,402$11.8M
avoro capital advisors llc2,849,402$9.8M
kvp capital advisors, lp2,165,997$7.5M
siren, l.l.c.2,082,000$7.2M
yu fan2,070,000$7.1M
stempoint capital lp1,878,738$6.5M
vanguard capital management llc1,315,770$4.5M

Showing top 10 of 62 institutional holders of Whitehawk Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 28, 2026
% of float
2.2%
Days to cover
4.0
Shares short
780,056
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

WHWK short interest

Governance

Frequently asked questions

What is the AI investment thesis for Whitehawk Therapeutics, Inc.?

Whitehawk Therapeutics, Inc. is a clinical-stage oncology company developing antibody-drug conjugates (ADCs) and has one marketed product, FYARRO (nab-sirolimus), for advanced PEComa.

What is Whitehawk Therapeutics, Inc.'s lead drug candidate?

Whitehawk Therapeutics, Inc.'s most advanced tracked candidate is fyarro (Phase 2) for Neuroendocrine tumors (NETs) of the GI tract, lung, or pancreas.

What is Whitehawk Therapeutics, Inc.'s next catalyst?

Whitehawk Therapeutics, Inc.'s next tracked catalyst is a Patent_Expiry event — "Patent_Expiry: NDA213312" — expected October 28, 2040.

Who is the CEO of Whitehawk Therapeutics, Inc.?

Dr. David J. Lennon Ph.D. is the chief executive officer of Whitehawk Therapeutics, Inc. (WHWK).

Where is Whitehawk Therapeutics, Inc. headquartered?

Whitehawk Therapeutics, Inc. (WHWK) is headquartered in Morristown, NJ, United States.

923 companies304,846 SEC filings22,682 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.