THE pipeline

One Platform. Multiple Indications. A Direct Path to the Clinic.

AlphaPARP is conducting pre-IND enabling studies with IND submission targeted for early 2027 with University of Pennsylvania conducting Phase 1 studies under Trevarx IND. First-in-human dosimetry studies are projected to begin in 2027.

programs

PARP1 Is Expressed Across the Solid Tumor Landscape

ProgramModalityTargetIndicationStage
AlphaPARPAlpha Therapy (²¹¹At)PARP1Ovarian Cancer, 
relapsed/refractoryIND-Enabling
Prostate Cancer (mCRPC)Preclinical
Breast Cancer (TNBC)Preclinical
NeuroblastomaPreclinical 
(Strong POC)
Pancreatic CancerExploratory
Small Cell Lung CancerExploratory
PARPTracePET Diagnostic (¹⁸F)PARP1Multiple tumor types, completing Phase 2 multi-center breast cancer trial300+ patients 
imaged

1ST MOVER ADVANTAGE

$21 Billion U.S. Total Addressable Market Across Initial and Expansion Indications

PARP1 is expressed across major solid tumor populations. The addressable market grows as the program advances through the indication ladder.

IndicationInitial TargetUltimate Target
OvarianPARPi-Resistant (~$1B)Stage 3/4 with 
PARP1 binding (~$2B)
ProstatemCRPC (~$7B)Same as Initial target
BreastTriple-Negative (~$4B)TNBC + ER+/HER- with 
PARP1 binding (~$12B)

U.S. total addressable market figures from the current investor pitch model.

THE NEAR TERM

From IND-Enabling to First-in-Human

Trevarx is currently completing IND-enabling work and CMC readiness for early clinical development. IND submission is targeted for early 2027 as a Trevarx IND to be conducted by University of Pennsylvania. First-in-human dosimetry studies are projected to begin in 2027 and Phase 1 dose escalation and expansion in relapsed/refractory ovarian cancer following.

The detailed development plan, milestone gates, and financing structure are reserved for the investor conversation. Use the contact form to request a briefing.

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Three Points to Take Away

(Based on public pipeline mapping)

Trevarx is the only identified IND-enabling targeted alpha program built for DNA-directed intranuclear delivery.

Most other named programs in development or approval focus on cell-surface, extracellular, or non-DNA-localized delivery.

The major alpha RLT acquirees and later-stage competitors largely compete on molecular target.

AlphaPARP reframes the competitive axis around delivery geometry: where the radiation fires relative to tumor DNA.

AlphaPARP uses Astatine-211, well matched to the small-molecule PARP-targeting scaffold.

Supply chain remains a known execution variable across the alpha RLT field, but Trevarx has a staged plan for early clinical supply, CMC development, and later network scale-up.

Talk to the Team About the Roadmap