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APVO

Aptevo Therapeutics Inc.

Pharmaceutical preparations·Phase 1·Seattle, WA, United States·CEO: Mr. Jeffrey G. Lamothe CA
Oncology

APVO evidence brief

What we can confirm

BioSniper Score:
5.1 / 10
Market Cap:
$3.3M
Lead Asset:
mipletamig (Phase 1)

What it means

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

What to watch

Market Cap: $3.3M · Lead Asset: mipletamig (Phase 1)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · APVO

Aptevo Therapeutics Inc. (APVO) is a clinical-stage biotechnology company developing novel multispecific immuno-oncology therapeutics based on its proprietary ADAPTIR and ADAPTIR-FLEX platforms, with lead candidate mipletamig in a Phase 1b/2 trial for frontline AML and a next-generation trispecific candidate, APVO451, expected to enter IND-enabling studies in H1 2027.

Key risk: Cash runway uncertainty

5.1/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$3.3M

Cash Runway

—

Lead Asset

mipletamig (Phase 1)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate for Aptevo Therapeutics Inc..

AI OverviewAI overview is shown in English only.

Aptevo Therapeutics Inc. (APVO) is a clinical-stage biotechnology company developing novel multispecific immuno-oncology therapeutics based on its proprietary ADAPTIR and ADAPTIR-FLEX platforms, with lead candidate mipletamig in a Phase 1b/2 trial for frontline AML and a next-generation trispecific candidate, APVO451, expected to enter IND-enabling studies in H1 2027.

  • Aptevo is a clinical-stage biotechnology company focused on developing novel immunotherapy candidates for cancer treatment [sec · filed 2026-08-21].
  • Lead clinical candidate mipletamig (CD123xCD3 T cell engager) is being evaluated in the RAINIER Phase 1b/2 trial for frontline AML in combination with venetoclax + azacitidine [sec_mda · as of 2026-08-14].
  • Cash & equivalents were $9.8M as of 2026-06-30, with net income of -$6.4M and shareholders' equity of $6.0M [sec].
  • Aptevo expects to enter IND-enabling studies for its lead trispecific candidate APVO451 in H1 2027 [news · published 2026-09-24].
  • The company has a 50/50 collaboration with Niowave to develop radiopharmaceutical oncology programs [news · published 2026-08-24].

What works

  • Aptevo's proprietary ADAPTIR and ADAPTIR-FLEX platforms enable rational design of precision immune modulatory drugs, supporting a pipeline of two clinical and six preclinical candidates [sec_mda · as of 2026-08-14].
  • Mipletamig's Phase 1 studies showed positive safety (no liver toxicity) and tolerability, with 58% of patients achieving a best response of stable disease [sec · filed 2026-08-21].
  • The company secured a $1.5 million non-dilutive grant to advance APVO451 and established a 50/50 collaboration with Niowave for radiopharmaceutical programs, indicating external validation and non-dilutive funding [news · published 2026-08-24].

What to weigh

  • Cash & equivalents of $9.8M as of 2026-06-30 may be insufficient to fund operations for at least one year, as the company itself notes existing cash resources are not expected to be sufficient [sec_mda · as of 2026-08-14].
  • Net income of -$6.4M as of 2026-06-30 reflects ongoing operating losses typical of a clinical-stage biotech with no approved products [sec].
  • The company faces numerous risks and uncertainties associated with research, development, and commercialization of pharmaceutical products, including potential delays in partnering and macroeconomic impacts [sec_mda · as of 2026-08-14].

From the filings

Quoted directly from source documents.

  • Aptevo is a clinical-stage biotechnology company developing novel immunotherapy candidates for cancer.

    “We are a clinical-stage, research and development biotechnology company focused on developing novel immunotherapy candidates for the treatment of different forms of cancer.”

    SEC filings · August 21, 2026

  • Mipletamig is being evaluated in the RAINIER Phase 1b/2 trial for frontline AML.

    “Clinical candidate mipletamig is a CD123xCD3 T cell engager currently being clinically evaluated in the RAINIER trial, part one of a Phase 1b/2 program initiated in August 2024 for the treatment of frontline acute myelogenous leukemia (AML) in combination with standard of care venetoclax + azacitidine.”

    SEC filings · August 14, 2026

  • Aptevo expects to enter IND-enabling studies for APVO451 in H1 2027.

    “Aptevo expects to enter Investigational New Drug ("IND") enabling studies for the lead candidate, APVO451, in 1H2027.”

    News · September 24, 2026

  • Cash resources are not expected to be sufficient to fund operations for at least one year.

    “our existing cash resources are not expected to be sufficient to fund operations for at least one year from the date the financial statements are issued.”

    SEC MD&A · August 14, 2026

Risks & what to watch (3)›

Key risks

  • Cash runway uncertainty — Cash of $9.8M as of 2026-06-30 may not sustain operations for one year; company itself states insufficiency [sec_mda · as of 2026-08-14].
  • No approved products — Net loss of -$6.4M as of 2026-06-30 reflects no revenue from product sales; all candidates are in clinical or preclinical stages [sec].
  • Clinical development risks — Numerous risks and uncertainties in R&D and commercialization; potential delays in partnering and macroeconomic impacts [sec_mda · as of 2026-08-14].

What to watch

  • Progress of mipletamig in the RAINIER Phase 1b/2 trial for frontline AML [sec_mda · as of 2026-08-14].
  • Initiation of IND-enabling studies for APVO451 in H1 2027 [news · published 2026-09-24].
  • Cash burn rate and any additional financing or partnership announcements given the limited cash runway [sec_mda · as of 2026-08-14].
  • Outcomes from the Niowave radiopharmaceutical collaboration [news · published 2026-08-24].

Sources: News · SEC filings · SEC MD&A · Generated October 8, 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 Health7.9

D/E 1.40 · 0% dilution

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Financials

Short Interest

as of May 20, 2026
% of float
7.8%
Days to cover
2.8
Shares short
92,205
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 →

APVO short interest

Governance

Frequently asked questions

What is the AI investment thesis for Aptevo Therapeutics Inc.?

Aptevo Therapeutics Inc. (APVO) is a clinical-stage biotechnology company developing novel multispecific immuno-oncology therapeutics based on its proprietary ADAPTIR and ADAPTIR-FLEX platforms, with lead candidate mipletamig in a Phase 1b/2 trial for frontline AML and a next-generation trispecific candidate, APVO451, expected to enter IND-enabling studies in H1 2027.

What is Aptevo Therapeutics Inc.'s lead drug candidate?

Aptevo Therapeutics Inc.'s most advanced tracked candidate is mipletamig (Phase 1) for frontline acute myelogenous leukemia (AML).

Who is the CEO of Aptevo Therapeutics Inc.?

Mr. Jeffrey G. Lamothe CA is the chief executive officer of Aptevo Therapeutics Inc. (APVO).

Where is Aptevo Therapeutics Inc. headquartered?

Aptevo Therapeutics Inc. (APVO) is headquartered in Seattle, WA, United States.

What therapeutic areas does Aptevo Therapeutics Inc. focus on?

Aptevo Therapeutics Inc. develops therapies across Oncology.

923 companies304,839 SEC filings22,636 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.