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INBX

Inhibrx Biosciences, Inc.

Biological products·Phase 2·La Jolla, CA, United States·CEO: Mr. Mark Paul Lappe
OncologyNephrology

INBX evidence brief

What we can confirm

BioSniper Score:
2.0 / 10
Market Cap:
$1.66B
Next Catalyst:
PDUFA · Apr 14, 2027

What it means

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

What to watch

Market Cap: $1.66B · Next Catalyst: PDUFA · Apr 14, 2027
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · INBX

Inhibrx Biosciences is a clinical-stage biotech developing ozekibart (INBRX-109) for chondrosarcoma and INBRX-106 for solid tumors, with a PDUFA date for ozekibart in April 2027 and a cash position of $133.3M as of 2026-06-30.

Key risk: Cash runway

2.0/10

BioSniper Score

Based on 2 of 6 signals

Limited data coverage

Market Cap

$1.66B

Cash Runway

—

Lead Asset

—

Financial data as of Jun 30, 2026.

Tracking 4 clinical trials · 1 catalyst for Inhibrx Biosciences, Inc..

AI OverviewAI overview is shown in English only.

Inhibrx Biosciences is a clinical-stage biotech developing ozekibart (INBRX-109) for chondrosarcoma and INBRX-106 for solid tumors, with a PDUFA date for ozekibart in April 2027 and a cash position of $133.3M as of 2026-06-30.

  • Cash & equivalents of $133.3M as of 2026-06-30 [sec].
  • Net income of -$36.6M and shareholders' equity of -$53.0M as of 2026-06-30 [sec].
  • Ozekibart (INBRX-109) has a PDUFA date of 2027-04-14 [catalyst].
  • INBRX-106 Phase 2/3 HexAgon-HN study in HNSCC started 2024-05-14; PFS data expected Q4 2026 [sec · filed 2026-05-11].
  • Accumulated deficit of $279.6M as of 2026-03-31 [sec_mda · as of 2026-05-14].

What works

  • Ozekibart has a defined PDUFA date (2027-04-14), providing a near-term regulatory catalyst [catalyst].
  • INBRX-106 showed promising early results with no treatment-related deaths and predominantly low-grade adverse events in the Phase 2 portion [sec · filed 2026-05-11].
  • The company has access to up to an additional $225.0 million in debt financing (Term C/D Loan) at the lenders' discretion [sec_mda · as of 2026-08-13].

What to weigh

  • Cash & equivalents of $133.3M as of 2026-06-30 may be limited relative to ongoing R&D and debt obligations [sec].
  • Shareholders' equity is negative (-$53.0M as of 2026-06-30), indicating liabilities exceed assets [sec].
  • The company has no revenue ($0.0M as of 2026-06-30) and relies entirely on financing and cash reserves [sec].
  • Accumulated deficit of $279.6M as of 2026-03-31 reflects sustained net losses [sec_mda · as of 2026-05-14].

From the filings

Quoted directly from source documents.

  • INBRX-106 Phase 2 safety profile

    “No treatment-related deaths were reported in either arm.”

    SEC filings · May 11, 2026

  • Accumulated deficit as of 2026-03-31

    “accumulated deficit of $279.6 million”

    SEC MD&A · May 14, 2026

Catalyst timeline

  • 2027-04-14 · PDUFA: ozekibart — FDA decision on ozekibart (INBRX-109) for unresectable or metastatic conventional chondrosarcoma.
Risks & what to watch (4)›

Key risks

  • Cash runway — Cash of $133.3M as of 2026-06-30 may be insufficient to fund operations to profitability without additional financing [sec].
  • Negative equity — Shareholders' equity of -$53.0M as of 2026-06-30 indicates liabilities exceed assets [sec].
  • No revenue — Total revenue of $0.0M as of 2026-06-30; company depends entirely on financing [sec].
  • Clinical trial risk — INBRX-106 Phase 3 data not yet available; PFS data expected Q4 2026 [sec · filed 2026-05-11].

What to watch

  • PDUFA decision for ozekibart on 2027-04-14 [catalyst].
  • INBRX-106 Phase 2 PFS data expected Q4 2026 [sec · filed 2026-05-11].
  • Initiation of Phase 3 portion of HexAgon study in Q3 2026 [sec · filed 2026-05-11].
  • Company's ability to draw down additional $225M debt financing [sec_mda · as of 2026-08-13].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated October 8, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 2 of 6 signals · derived from public data

Pipeline inputs are unavailable for this score. It uses only the available signals shown below.

Cash RunwayN/A

Cash runway data unavailable

Financial Health2.0

Net income -$37M

Pipeline MaturityN/A

No tracked pipeline phase

Pipeline BreadthN/A

No tracked pipeline candidates

Catalyst Momentum2.0

1 upcoming, next in ~182d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Regulatory

Financials

Short Interest

as of Apr 20, 2026
% of float
19.9%
Days to cover
10.2
Shares short
2,119,421
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 →

INBX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Inhibrx Biosciences, Inc.?

Inhibrx Biosciences is a clinical-stage biotech developing ozekibart (INBRX-109) for chondrosarcoma and INBRX-106 for solid tumors, with a PDUFA date for ozekibart in April 2027 and a cash position of $133.3M as of 2026-06-30.

What is Inhibrx Biosciences, Inc.'s next catalyst?

Inhibrx Biosciences, Inc.'s next tracked catalyst is a PDUFA event — "PDUFA: ozekibart" — expected April 14, 2027.

Who is the CEO of Inhibrx Biosciences, Inc.?

Mr. Mark Paul Lappe is the chief executive officer of Inhibrx Biosciences, Inc. (INBX).

Where is Inhibrx Biosciences, Inc. headquartered?

Inhibrx Biosciences, Inc. (INBX) is headquartered in La Jolla, CA, United States.

What therapeutic areas does Inhibrx Biosciences, Inc. focus on?

Inhibrx Biosciences, Inc. develops therapies across Oncology, Nephrology.

923 companies304,844 SEC filings22,644 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.