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Floatz Rating
B58/100
Confidence
Indicative
v0.2
Sponsor
GlaxoSmithKline
Modality
monoclonal_antibody
Development Phase
Phase 2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
54High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
A Study of GSK5764227 in Participants With Advanced Solid Tumors (EMBOLD)
Recruiting
Study of EO-3021 in Adult Patients With Solid Tumors Likely to Express CLDN18.2
Terminated
First-Time-in-Human Study of GSK4381562 in Participants With Advanced Solid Tumors
Active Not Recruiting
Platform Trial of Novel Regimens Versus Standard of Care (SoC) in Participants With Non-small Cell Lung Cancer (NSCLC) - Sub-study 3
Completed
Dose Escalation and Cohort Expansion Study of Niraparib and Dostarlimab in Paediatric Participants With Solid Tumors (SCOOP)
Terminated
Study of the Safety and Effectiveness of GSK6097608 in Participants With Advanced Solid Tumors
Active Not Recruiting
Study of Induction PD-1 Blockade in Subjects With Locally Advanced Mismatch Repair Deficient Solid Tumors
Recruiting
A First Time in Human (FTIH) Study of GSK3745417 Administered to Participants With Advanced Solid Tumors
Active Not Recruiting
Platform Trial of Novel Regimens Versus Standard of Care (SoC) in Participants With Non-small Cell Lung Cancer (NSCLC)
Completed
Study of Niraparib, TSR-022, Bevacizumab, and Platinum-Based Doublet Chemotherapy in Combination With TSR-042
Completed
Show 5 more trials
Effects of Single Agent Niraparib and Niraparib Plus Programmed Cell Death-1 (PD-1) Inhibitors in Non-Small Cell Lung Cancer Participants
Completed
Study of TSR-033 With an Anti-programmed Cell Death-1 Receptor (PD-1) in Participants With Advanced Solid Tumors
Completed
A Study of TSR-022 in Participants With Advanced Solid Tumors (AMBER)
Active Not Recruiting
Dose Escalation and Expansion Study of GSK3359609 in Participants With Selected Advanced Solid Tumors (INDUCE-1)
Completed
Study of TSR-042, an Anti-programmed Cell Death-1 Receptor (PD-1) Monoclonal Antibody, in Participants With Advanced Solid Tumors
Active Not Recruiting

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
Dostarlimab (this asset)GlaxoSmithKlineP2B · 58
PanitumumabAstellas Pharma IncP2BBB
Granulocyte Colony-Stimulating Factor LenograstimSanofiP4BB
DexmedetomidineMedical College of WisconsinP4BB
LidocaineMedical College of WisconsinP4BB
RelatlimabBristol-Myers SquibbP2BB
Vitamin DTanta UniversityP4BB
GlycopyrrolateMedical College of WisconsinP4BB
Dinitrogen MonoxideMedical College of WisconsinP4BB

+42 more in the Neoplasm cohort

Other indications for Dostarlimab

IndicationSponsorPhaseRating
Non-Small Cell Lung CarcinomaP3BB · 68
Ovarian CarcinomaP3BB · 65
Colonic NeoplasmP3B · 60

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. Dostarlimab in Neoplasm. Methodology v0.2.
Rated under v0.2 effective July 8, 2026. Last refreshed July 8, 2026.
Accessed July 14, 2026.
https://terminal.floatz.ai/assets/dostarlimab-neoplasm

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