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Retifanlimab

Human Papillomavirus-Related Squamous Cell Carcinoma

Explore 17 assets in Human Papillomavirus-Related Squamous Cell Carcinoma
Floatz Rating
CCC53/100
Confidence
Indicative
v0.2
Sponsor
Jennifer Dorth
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.
38Indicative
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
ctHPVDNA Response-Adapted Chemoradiation +/- Retifanlimab Treatment in Locally-Advanced Anal Cancer
Not Yet Recruiting

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
81High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Human Papillomavirus-Related Squamous Cell Carcinoma

AssetSponsorPhaseRating
Retifanlimab (this asset)Jennifer DorthP2CCC · 53
CyclophosphamideChristian HinrichsP2B
FludarabineChristian HinrichsP2B
e7 tcr-t cellsChristian HinrichsP2B
9-valent human papillomavirus recombinant vaccineShanghai Bovax Biotechnology Co., Ltd.P3B
scg142SCG Cell Therapy Pte. Ltd.P1/2CCC
RegorafenibInstitut BergoniéP1/2CC
AlpelisibPamela MunsterP1CC
scg142 tcr-t cellsThe Affiliated Hospital of Qingdao UniversityP1CC

+10 more in the Human Papillomavirus-Related Squamous Cell Carcinoma cohort

Other indications for Retifanlimab

IndicationSponsorPhaseRating
Anal Canal Squamous Cell CarcinomaP3BB · 66
Urothelial CarcinomaP2BB · 66
Renal Cell CarcinomaP2B · 63

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. Retifanlimab in Human Papillomavirus-Related Squamous Cell Carcinoma. 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/retifanlimab-human-papillomavirus-related-squamous-cell-carcinoma

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