Floatz logo
Floatz Rating
B62/100
Confidence
Indicative
v0.2
Sponsor
The First Affiliated Hospital of Soochow University
Modality
Small molecule
Development Phase
Phase 3
Status
Active
Evidence ledger · v0.2

Clinical Evidence

Clinical track record: trial progression, reported outcomes, safety signals, and endpoint quality.
61High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Polatuzumab Vedotin and Zanubrutinib Plus R-CHP for Patients With Newly Diagnosed Untreated Non-GCB DLBCL
Enrolling By Invitation
NEROFE and Doxorubicin in KRAS-mutated ST2-positive Solid Tumors
Recruiting
A Pilot Study of Thermodox and MR-HIFU for Treatment of Relapsed Solid Tumors
Withdrawn
A Phase 2 Study of Isatuximab in Combination With Bortezomib, Cyclophosphamide and Dexamethasone Followed by Isatuximab and Lenalidomide Maintenance in Newly Diagnosed Patients With Multiple Myeloma and Severe Renal Impairment
Unknown
The Neoadjuvant Combined Hormone Therapy in Premenopausal Women With Locally Advanced ER+/HER2- Breast Cancer
Unknown
A Study of Azenosertib (ZN-c3) in Patients With Ovarian Cancer
Recruiting
A Study Evaluating the Safety, Tolerability, Pharmacokinetics and Preliminary Activity of Idasanutlin in Combination With Either Chemotherapy or Venetoclax in Treatment of Pediatric and Young Adult Participants With Relapsed/Refractory Acute Leukemias or Solid Tumors
Terminated
A Study of E7386 in Combination With Other Anticancer Drug(s) in Participants With Solid Tumor
Active Not Recruiting
A Study of TRK-950 in Combinations With Anti-Cancer Treatment Regimens in Patients With Advanced Solid Tumors
Active Not Recruiting
9-ING-41 in Patients With Advanced Cancers
Active Not Recruiting
Show 28 more trials
Chidamide Combined With CHOPE Regimen for Peripheral T-cell Lymphoma Patients
Unknown
A Phase I Study of Lyso-thermosensitive Liposomal Doxorubicin and MR-HIFU for Pediatric Refractory Solid Tumors
Terminated
Phase I Study of MLN0128 and MLN8237 in Patients With Advanced Solid Tumors and Metastatic Triple-negative Breast Cancer
Completed
A Study of Olaratumab in Japanese Participants With Advanced Cancer
Completed
Pharmacokinetic Study of Docetaxel-PNP and Taxotere to Treat Patient With Advanced Solid Cancer
Completed
COPANLISIB (BAY80-6946) Drug-drug Interaction and Cardiovascular Safety Study in Advanced Solid Tumor and Non-Hodgkin's Lymphoma Patients
Completed
Effects of STM 434 Alone or in Combination With Liposomal Doxorubicin in Patients With Ovarian Cancer or Other Advanced Solid Tumors
Completed
An Open-Label Study of a Novel JAK-inhibitor, INCB052793, Given to Patients With Advanced Malignancies
Terminated
A Study of DOXIL/CAELYX in Patients With Advanced or Refractory Solid Malignancies Including Patients With Ovarian Cancer
Completed
Combination of Hyperthermia and Concurrent Chemoradiotherapy (CCRT) in Treatment Failure Solid Tumors
Withdrawn
Safety, Tolerability and Pharmacokinetic (PK) of Concomitant Esomeprazole and Rifampin, and QT Study on Single and Multiple-doses of Alisertib
Completed
A Pivotal Bioequivalence Study of DOXIL/CAELYX (Doxorubicin HCL) in Patients With Advanced or Refractory Solid Malignancies Including Patients With Ovarian Cancer
Completed
Single Dose of Intravenous rhTNF-α and Liposomal Doxorubicin in Patients With Advanced Solid Tumors or Lymphomas
Withdrawn
Treatment Extension Study for Patients Who Have Previously Participated and Have Benefited From Iniparib in a Clinical Trial
Completed
Phase I Study of PI3(Phosphoinositol 3)-Kinase Inhibitor BAY80-6946 With Paclitaxel in Patients With Advanced Cancer
Completed
Study of Anti-HB-EGF Antibody KHK2866 in Subjects With Advanced Solid Tumors and Ovarian Cancer
Terminated
A Study of Robatumumab (SCH 717454, MK-7454) in Combination With Different Treatment Regimens in Pediatric Participants With Advanced Solid Tumors (P05883, MK-7454-006)
Terminated
Pharmacokinetic Study of SYP-0704A and Taxotere to Treat Patient With Advanced Solid Cancer
Completed
Multiple Ascending Dose (MAD) Combination in Subjects With Multiple Myeloma
Completed
AZD2281 in Combination With Liposomal Doxorubicin in Advanced Solid Tumours
Terminated
AMG386 Comb w. Either Pegylated Liposomal Doxorubicin or Topotecan Subjects w. Advanced Recurrent Epithelial Ovarian CR
Completed
Dose-Escalation Study of LY573636-sodium and Liposomal Doxorubicin in Patients With Advanced Solid Tumors
Completed
Study of Pegylated Human Recombinant Arginase for Liver Cancer
Completed
Anti-EGFR Immunoliposomes in Solid Tumors
Completed
Breast Cancer Treated by Neoadjuvant Chemotherapy
Completed
AMG 531 in Patients With Advanced Malignancy Receiving Treatment With Carboplatin
Completed
Doxil, Gemcitabine, and Velcade (PS341) in Advanced Cancer Patients
Completed
Taxotere, Cisplatin, and CPT-11 in Advanced Solid Tumor Malignancies
Completed

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
Adriamycin (this asset)The First Affiliated Hospital of Soochow UniversityP3B · 62
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 Adriamycin

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. Adriamycin 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/adriamycin-neoplasm-20647

Need depth?

Order a full diligence report on this asset.

Order report →

Are you the sponsor?

Submit your data room for a Verified Rating. The public-data rating remains visible alongside.

Contact →