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CATX

Perspective Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 1·Seattle, WA, United States·CEO: Mr. Johan M. Spoor
OncologyDermatology

CATX evidence brief

What we can confirm

BioSniper Score:
7.2 / 10
Market Cap:
$320.8M
Lead Asset:
PSV359 (Phase 1/Phase 2)

What it means

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

What to watch

Market Cap: $320.8M · Lead Asset: PSV359 (Phase 1/Phase 2)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CATX

Perspective Therapeutics (CATX) is a clinical-stage radiopharmaceutical company developing targeted alpha-particle therapies using Lead-212 for multiple oncology indications, with a lead program advancing toward Phase 3.

Key risk: No approved products

7.2/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$320.8M

Cash Runway

—

Lead Asset

PSV359 (Phase 1/Phase 2)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 3 clinical trials for Perspective Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Perspective Therapeutics (CATX) is a clinical-stage radiopharmaceutical company developing targeted alpha-particle therapies using Lead-212 for multiple oncology indications, with a lead program advancing toward Phase 3.

  • Cash, cash equivalents, and short-term investments were approximately $237 million as of June 3, 2026 [news].
  • Net income was -$26.8M and shareholders' equity was $323.9M as of 2026-06-30 [sec].
  • Lead program VMT-α-NET is advancing toward a Phase 3 study in neuroendocrine tumors, with clinical site activation targeted around year-end 2026 subject to regulatory feedback [news].
  • Announced a clinical collaboration with Merck to evaluate [212Pb]PSV359 in combination with Keytruda in FAP-α positive solid tumors [news].
  • The company has not generated revenue from product sales other than its discontinued brachytherapy business and has incurred significant net losses [sec_mda].

What works

  • Strong cash position of approximately $237 million as of June 3, 2026 provides runway to fund clinical milestones into late 2027 [news][sec_mda].
  • Proprietary Lead-212 alpha-emitting platform enables a theranostic approach that may improve efficacy and minimize toxicity [sec_mda].
  • Multiple clinical-stage programs (VMT-α-NET, VMT01, PSV359) diversify pipeline risk and target different tumor types [pipeline][news].
  • Clinical collaboration with Merck for PSV359 plus Keytruda adds validation and potential combination therapy upside [news].

What to weigh

  • No regulatory approval for any current product candidate; the company has not generated revenue from product sales other than its discontinued brachytherapy business [sec_mda].
  • Recurring net losses, with a net loss of -$26.8M reported as of 2026-06-30 [sec].
  • Expenses are expected to increase as clinical programs advance, requiring continued capital and no guarantee of future funding [sec_mda].
  • VMT-α-NET faces competition from Lutathera (Novartis) in the neuroendocrine tumor space [pipeline].

From the filings

Quoted directly from source documents.

  • Cash position as of June 3, 2026

    “Approximately $237 million in cash, cash equivalents, and short-term investments as of June 3”

    News · August 10, 2026

  • No revenue from product sales other than discontinued brachytherapy business

    “have not generated any revenue from product sales other than our discontinued brachytherapy business and have incurred significant net losses”

    SEC MD&A · March 16, 2026

  • VMT-α-NET Phase 3 planning

    “Advancing VMT-α-NET toward a Phase 3 study in neuroendocrine tumors, subject to regulatory alignment: regulatory engagement ongoing; clinical site activation targeted around year-end 2026 subject to regulatory feedback”

    News · August 10, 2026

Catalyst timeline

  • 2023-06-01 · Phase 2 start for VMT01 melanoma study — First-in-human study of [212Pb]VMT01 in melanoma initiated.
  • 2023-09-27 · Phase 2 start for VMT-α-NET NET study — First-in-human study of [212Pb]VMT-α-NET in SSTR2-positive tumors initiated.
  • 2025-04-28 · Phase 2 start for PSV359 FAP study — First-in-human study of [203/212Pb]PSV359 in FAP-positive solid tumors initiated.
Risks & what to watch (4)›

Key risks

  • No approved products — No regulatory approval for any current product candidate; no revenue from product sales other than discontinued brachytherapy [sec_mda].
  • Recurring net losses — Net loss of -$26.8M as of 2026-06-30; expenses expected to increase with clinical advancement [sec][sec_mda].
  • Competition in NET space — VMT-α-NET competes with Lutathera (Novartis) in neuroendocrine tumors [pipeline].
  • Dependence on future capital — Company has limited operating history and may need additional capital to fund operations beyond late 2027 [sec_mda].

What to watch

  • Regulatory alignment and clinical site activation for VMT-α-NET Phase 3 study, targeted around year-end 2026 [news].
  • Oral presentation of VMT-α-NET study update at ESMO 2026 [news].
  • Progress of the Merck collaboration for PSV359 plus Keytruda in FAP-α positive solid tumors [news].
  • Cash burn rate and any future capital raises as expenses increase [sec_mda].

Sources: Catalysts · News · Pipeline · SEC MD&A · Generated October 9, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.7

D/E 0.21 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

136

Total value held

$350.7M

HolderSharesValue
avidity partners management lp12,099,998$48.8M
tcg crossover management, llc7,915,567$33.0M
commodore capital lp6,336,782$26.4M
blackrock, inc.5,348,561$22.3M
opaleye management inc.4,675,000$19.5M
vanguard capital management llc4,378,956$18.3M
millennium management llc4,046,640$16.9M
citadel advisors llc3,566,504$14.9M
affinity asset advisors, llc3,164,582$13.2M
state street corp3,132,670$13.1M

Showing top 10 of 136 institutional holders of Perspective Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
13.6%
Days to cover
11.1
Shares short
12,997,351
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 →

CATX short interest

Governance

Frequently asked questions

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

Perspective Therapeutics (CATX) is a clinical-stage radiopharmaceutical company developing targeted alpha-particle therapies using Lead-212 for multiple oncology indications, with a lead program advancing toward Phase 3.

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

Perspective Therapeutics, Inc.'s most advanced tracked candidate is PSV359 (Phase 1/Phase 2) for Pancreatic Ductal Adenocarcinoma.

Who is the CEO of Perspective Therapeutics, Inc.?

Mr. Johan M. Spoor is the chief executive officer of Perspective Therapeutics, Inc. (CATX).

Where is Perspective Therapeutics, Inc. headquartered?

Perspective Therapeutics, Inc. (CATX) is headquartered in Seattle, WA, United States.

What therapeutic areas does Perspective Therapeutics, Inc. focus on?

Perspective Therapeutics, Inc. develops therapies across Oncology, Dermatology.

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.