Skip to main content
CMPXNasdaq

Compass Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 3·Boston, MA, United States·CEO: Dr. Thomas J. Schuetz M.D., Ph.D.
OncologyNephrology

CMPX evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

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

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CMPX

Compass Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing bispecific antibodies for oncology, with lead programs CTX-009, CTX-471, and CTX-8371 in Phase 1/2/3 trials and a novel PD-1/VEGF bispecific CTX-10726 entering the clinic.

Key risk: No approved products

8.7/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$432.2M

Cash Runway

35.3 mo

Financial data as of Jun 30, 2026.

Tracking 6 pipeline candidates · 6 clinical trials · 2 catalysts for Compass Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Compass Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing bispecific antibodies for oncology, with lead programs CTX-009, CTX-471, and CTX-8371 in Phase 1/2/3 trials and a novel PD-1/VEGF bispecific CTX-10726 entering the clinic.

  • As of June 30, 2025, Compass had $101 million in cash, cash equivalents and marketable securities, expected to fund operations into 2027 [sec_mda · as of 2025-08-11].
  • The company has incurred significant operating losses, with a net loss of $16.6 million for Q1 2025 and an accumulated deficit of $381.3 million as of March 31, 2025 [sec_mda · as of 2025-05-08].
  • Lead programs include CTX-009 (Phase 2/3), CTX-471 (Phase 2), and CTX-8371 (Phase 1a), with a novel PD-1/VEGF bispecific CTX-10726 expected to file an IND in Q4 2025 and announce clinical data in 2026 [sec_mda · as of 2024-11-12][sec_mda · as of 2025-08-11].
  • Compass has raised $430 million in gross proceeds from equity sales through June 30, 2025, and expects to require additional financing to complete development [sec_mda · as of 2025-08-11].
  • The company faces risks common to pre-revenue biotechs: no approved products, reliance on future financing, and dependence on successful clinical trials and regulatory approvals [sec_mda · as of 2025-02-27].

What works

  • Compass has a diversified pipeline of bispecific antibodies targeting multiple oncology pathways, including CTX-009 (DLL4/VEGF), CTX-471 (CD137), CTX-8371 (PD-1/PD-L1), and CTX-10726 (PD-1/VEGF), providing multiple shots on goal [sec_mda · as of 2025-08-11].
  • The company has demonstrated ability to raise capital, with $430 million in gross equity proceeds through June 2025, and has a cash runway into 2027 based on current plans [sec_mda · as of 2025-08-11].
  • CTX-10726 was discovered in-house and leverages existing components from tovecimig and CTX-8371, potentially enabling faster development and commercial-scale manufacturing yields [sec_mda · as of 2025-08-11].

What to weigh

  • Compass has no approved products and has never generated product revenue; it expects to continue incurring significant losses for at least several more years [sec_mda · as of 2025-05-08].
  • The company will require substantial additional financing to complete development and commercialization, and may be unable to raise funds on favorable terms or at all [sec_mda · as of 2025-02-27].
  • Cash runway estimates are based on assumptions that may prove wrong, and the company could exhaust capital sooner than expected, potentially forcing delays or reductions in development [sec_mda · as of 2025-08-11].
  • Clinical and regulatory success is uncertain; delays in trials, manufacturing, or FDA interactions could materially impact timelines and financial position [sec_mda · as of 2025-02-27].

From the filings

Quoted directly from source documents.

  • Cash position and runway into 2027

    As of June 30, 2025, we had $101 million in cash, cash equivalents and marketable securities. We expect that such cash resources will enable us to fund our operating expenses and capital expenditure requirements into 2027.

    SEC MD&A · August 11, 2025

  • Accumulated deficit and net loss

    Our net losses were $16.6 million and $10.8 million for the three months ended March 31, 2025 and 2024, respectively. We had an accumulated deficit of $381.3 million on March 31, 2025.

    SEC MD&A · May 8, 2025

  • Need for additional financing

    We will require substantial additional financing to pursue our business objectives, which may not be available on acceptable terms, or at all.

    SEC MD&A · February 27, 2025

Catalyst timeline

  • 2026-09-01 · Phase 2 Start: CTX-471 in NCAM Positive TumorsInitiation of a Phase 2 open-label study of CTX-471 in patients with NCAM-positive tumors; will provide initial efficacy and safety data.
  • 2026-12-01 · Phase 3 Topline: CTX-009 + Paclitaxel vs PaclitaxelTopline results from a Phase 2/3 randomized controlled study of CTX-009 in combination with paclitaxel; pivotal data for potential registration.
Risks & what to watch (4)

Key risks

  • No approved productsCompass has no products approved for commercial sale and has never generated product revenue [sec_mda · as of 2025-05-08].
  • Financing dependencyThe company will need substantial additional capital to complete development; failure to raise funds could force delays or termination of programs [sec_mda · as of 2025-02-27].
  • Clinical trial risksDelays in patient enrollment, manufacturing, or regulatory interactions could materially impact timelines and financial position [sec_mda · as of 2025-02-27].
  • Competitive landscapeThe oncology and immunology market is highly competitive, with many emerging therapies that could limit commercial potential [sec_mda · as of 2026-03-05].

What to watch

  • Initiation of the Phase 2 study for CTX-471 in NCAM-positive tumors, expected to start September 2026 [upcoming catalysts].
  • Topline data from the Phase 2/3 study of CTX-009 in combination with paclitaxel, expected December 2026 [upcoming catalysts].
  • IND submission for CTX-10726 in Q4 2025 and clinical data announcement expected in 2026 [sec_mda · as of 2025-08-11].
  • Cash runway updates; as of June 30, 2025, cash of $101 million was expected to fund operations into 2027 [sec_mda · as of 2025-08-11].

Sources: SEC MD&A · Generated August 29, 2026 · How we verify sources →

Run Compass Therapeutics, Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Compass Therapeutics, Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway9.8

35.3 months

Financial Health9.6

D/E 0.15

Pipeline Maturity8.5

Lead: Phase 2/Phase 3

Pipeline Breadth9.8

6 candidates

Catalyst Momentum6.0

2 upcoming, next in ~2d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

202

Total value held

$918.3M

HolderSharesValue
tang capital management llc16,790,809$88.8M
orbimed advisors llc15,219,994$80.5M
suvretta capital management, llc14,307,379$75.7M
vanguard capital management llc12,074,350$63.9M
blackrock, inc.9,506,080$50.3M
adage capital partners gp, l.l.c.8,486,500$44.9M
enavate sciences gp, llc7,788,150$41.2M
bvf inc/il7,764,842$41.1M
state street corp6,694,976$35.4M
rtw investments, lp4,186,599$22.1M

Showing top 10 of 202 institutional holders of Compass Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
20.2%
Days to cover
2.4
Shares short
30,416,716
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 →

CMPX short interest

Governance

Frequently asked questions

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

Compass Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing bispecific antibodies for oncology, with lead programs CTX-009, CTX-471, and CTX-8371 in Phase 1/2/3 trials and a novel PD-1/VEGF bispecific CTX-10726 entering the clinic.

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

Compass Therapeutics, Inc.'s most advanced tracked candidate is CTX-009 (Phase 2) for Biliary Tract Cancer; Metastatic Colorectal Cancer.

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

Compass Therapeutics, Inc.'s next tracked catalyst is a Phase2_Start event — "Phase 2 Start: A Phase 2, Open-Label Study of CTX-471 in Patients With NCAM Positive Tumors" — expected September 1, 2026.

Who is the CEO of Compass Therapeutics, Inc.?

Dr. Thomas J. Schuetz M.D., Ph.D. is the chief executive officer of Compass Therapeutics, Inc. (CMPX).

Where is Compass Therapeutics, Inc. headquartered?

Compass Therapeutics, Inc. (CMPX) is headquartered in Boston, MA, United States.

925 companies232,681 SEC filings21,419 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.