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Sumoylation Inhibitor Tak-981

Neoplasm

Explore 889 assets in Neoplasm
Floatz Rating
D29/100
Confidence
Indicative
v0.2Rating updated July 14, 2026
Sponsor
Takeda
Modality
Small molecule
Development Phase
Phase 1/2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
17High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
An Absorption, Distribution, Metabolism, Excretion (ADME) Study of [14C]Subasumstat in Adults With Advanced or Metastatic Solid Tumors
Terminated
A Study of TAK-981 in People With Advanced Solid Tumors or Cancers in the Immune System
Terminated

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
65High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Neoplasm

AssetSponsorPhaseRating
Sumoylation Inhibitor Tak-981 (this asset)TakedaP1/2D · 29
PanitumumabAstellas Pharma IncP2BB
IrinotecanMirati Therapeutics Inc.P4BB
NivestimAnkara Etlik City HospitalP2BB
DexasoneHellenic Society of HematologyP3BB
FeladilimabGlaxoSmithKlineP2BB
Pralsetinib, Trans-Seoul National University Bundang HospitalP3BB
CarboplatinBristol-Myers SquibbP3BB
Granulocyte Colony-Stimulating Factor LenograstimSanofiP4BB

+42 more in the Neoplasm cohort

Other indications for Sumoylation Inhibitor Tak-981

IndicationSponsorPhaseRating
Plasma Cell MyelomaP1/2D · 28
Hematopoietic And Lymphoid System NeoplasmP1/2D · 28
Non-Hodgkin LymphomaP1/2D · 28

Scientific Foundation

Strength of the underlying biology: target validation, tractability, modality fit, and how related mechanisms have fared.
NR

Planned for methodology v0.2.

Development Feasibility

How realistically the program can be executed, drawing on modality precedent, enrollment dynamics, and sponsor delivery.
NR

Planned for methodology v0.2.

Commercial Opportunity

Commercial prize: addressable population, unmet need, and the value case for the indication.
NR

Planned for methodology v0.2.

IP & Exclusivity

Exclusivity position, covering patent protection and freedom-to-operate runway.
NR

Planned for methodology v0.2.

Manufacturing & Supply

Manufacturing and supply readiness, driven by modality process and scale-up risk.
NR

Planned for methodology v0.2.

Related assets

Citation

Floatz Terminal. Sumoylation Inhibitor Tak-981 in Neoplasm. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 14, 2026.
Accessed July 15, 2026.
https://terminal.floatz.ai/assets/sumoylation-inhibitor-tak-981-neoplasm-111882

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