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Floatz Rating
CCC55/100
Confidence
Indicative
v0.2
Sponsor
Asan Medical Center
Modality
Small molecule
Development Phase
Phase 2
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
52High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
KPMNG Study of MOlecular Profiling Guided Therapy Based on Genomic Alterations in Advanced Solid Tumors II
Recruiting
A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-6036 Alone or in Combination in Participants With Advanced or Metastatic Solid Tumors With a KRAS G12C Mutation
Active Not Recruiting
A Study of LY3499446 in Participants With Advanced Solid Tumors With KRAS G12C Mutation
Terminated
Canadian Profiling and Targeted Agent Utilization Trial (CAPTUR)
Recruiting
Itacitinib in Combination With Erlotinib in Non Small Cell Lung Cancer Patients With Epidermal Growth Factor Receptor (EGFR) Activating Mutations
Withdrawn
A Rollover Study for Subjects That Have Participated in an Astellas Sponsored Linsitinib Trial
Completed
A Study to Evaluate Foretinib in Subjects With Non-Small-Cell Lung Cancer
Withdrawn
Erlotinib in Combination With Pralatrexate in Advanced Malignancies
Completed
Study of ABT-700 in Subjects With Advanced Solid Tumors
Completed
Determination of Intratumoral Concentrations of Kinase Inhibitors in Patients With Advanced Solid Malignancies.
Completed
Show 9 more trials
Safety and Tolerability Study of GSK1120212, a MEK Inhibitor, in Combination With Docetaxel, Erlotinib, Pemetrexed, Pemetrexed + Carboplatin, Pemetrexed + Cisplatin, or Nab-Paclitaxel
Completed
Hormone Receptor Positive Disease Across Solid Tumor Types: A Phase I Study of Single-Agent Hormone Blockade and Combination Approaches With Targeted Agents to Provide Synergy and Overcome Resistance
Completed
Study to Evaluate Panobinostat (DACi) Pharmacokinetics and Safety in Solid Tumors and Varying Renal Function
Completed
A Phase 1 Dose-escalation Study of OSI-906 and Erlotinib (Tarceva®)
Completed
Safety Study of XL765 (SAR245409) in Combination With Erlotinib in Adults With Solid Tumors
Completed
A Safety Study in Participants With Advanced Solid Tumors
Terminated
LBH589 Oral in Combination With Carboplatin and Paclitaxel in Advanced Solid Tumors
Unknown
Safety Study of XL147 (SAR245408) in Combination With Erlotinib in Adults With Solid Tumors
Completed
Phase I Study of Indibulin in Combination With Erlotinib in Advanced Solid Tumors
Unknown

Competitive Position

Competitive setting: how crowded the indication is, class-level failures, and timing against rivals.
59High confidence
Detailed axis rationale is planned and will be published soon.

Same indication · Cancer

AssetSponsorPhaseRating
Panobinostat (this asset)Asan Medical CenterP2CCC · 55
NabiximolsJazz PharmaceuticalsP3BBB
PyridoxolM.D. Anderson Cancer CenterP4BB
RivoceranibJiangsu HengRui Medicine Co., Ltd.P4BB
DesfluranePeter MacCallum Cancer Centre, AustraliaP4BB
PropofolHong Kong Children's HospitalP4BB
EpirubicinZhejiang Provincial People's HospitalP3BB
AtorvastatinCancer Institute and Hospital, Chinese Academy of Medical SciencesP2/3BB
AnamorelinHelsinn Healthcare SAP3BB

+42 more in the Cancer cohort

Other indications for Panobinostat

IndicationSponsorPhaseRating
Hodgkins LymphomaP3BB · 68
Chronic Lymphocytic Leukemia/Small Lymphocytic LymphomaP2BB · 66
Mantle Cell LymphomaP2BB · 66

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. Panobinostat in Cancer. 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/panobinostat-cancer

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