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Floatz Rating
CCC55/100
Confidence
Indicative
v0.2
Sponsor
Eli Lilly and Company
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.
45Indicative
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 or IDH2 Mutations
Active Not Recruiting
Study of Olaparib and Durvalumab in IDH-Mutated Solid Tumors
Recruiting

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
73High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Glioma

AssetSponsorPhaseRating
Durvalumab (this asset)Eli Lilly and CompanyP2CCC · 55
OlutasidenibRigel PharmaceuticalsP4BBB
IrinotecanKailin Yang, MD, PhDP3B
DianhydrogalactitolKintara Therapeutics, Inc.P2B
CyclophosphamideEssen BiotechP2B
Valproic AcidMedical University of South CarolinaP2B
NivolumabJason J. Luke, MDP2B
CamustineUniversity of California, DavisP3B
CarboplatinDelMar Pharmaceuticals, Inc.P3B

+42 more in the Glioma cohort

Other indications for Durvalumab

IndicationSponsorPhaseRating
Ovarian CarcinomaP2BB · 70
Primary Peritoneal CarcinomaP2BB · 70
Urothelial CarcinomaP3BB · 70

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. Durvalumab in Glioma. 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/durvalumab-glioma

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