Floatz logo
Floatz Rating
B62/100
Confidence
Indicative
v0.2
Sponsor
InSilico Medicine Hong Kong Limited
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.
63High confidence
Detailed axis rationale is planned and will be published soon.
TrialPhaseStatusNPrimary endpointReadout
Study of ISM5939 in Patients With Advanced and/or Metastatic Solid Tumors
Not Yet Recruiting
Neoadjuvant CAPEOX Versus Upfront Surgery for Locally Advanced Colon Cancer With Elevated CEA: A Single-Center, Open-Label, Randomized Controlled Trial
Not Yet Recruiting
A Phase I/II Study of LM-2417 in Subjects With Advanced Solid Tumours
Recruiting
A Clinical Trial of LBL-024 Combination Drug in Patients With Advanced Solid Tumours[Substudy 01(NSCLC)]
Recruiting
AK129 Combination Therapy for Advanced Solid Tumors
Recruiting
A Study of QLM2011 in Subjects With Advanced Solid Tumors
Not Yet Recruiting
A Phase I/II Study of CS2009 in Participants With Advanced Solid Tumors
Recruiting
A Study Assessing KB707 for the Treatment of Advanced Solid Tumor Malignancies Affecting the Lungs
Recruiting
A Study of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies
Active Not Recruiting
A Study of KK2269 in Adult Participants With Solid Tumors
Recruiting
Show 65 more trials
FT825/ONO-8250, an Off-the-Shelf, HER2 CAR-T, With or Without Monoclonal Antibodies in Advanced Solid Tumors
Recruiting
A Study of ASKG915 in Patients With Selected Advanced Solid Tumors.
Recruiting
A First-in-Human (FIH) Study to Evaluate the Safety and Tolerability of VVD-130037 in Participants With Advanced Solid Tumors
Recruiting
PRT3789 Monotherapy and in Combo w/Docetaxel in Participants w/Advanced or Metastatic Solid Tumors w/SMARCA4 Mutation
Completed
NUC-3373 in Combination With Other Agents in Patients With Advanced Solid Tumours
Terminated
A Study of BMS-986360/CC-90001 Alone and in Combination With Chemotherapy or Nivolumab in Advanced Solid Tumors
Completed
SKB264 Monotherapy in Selected Subjects With Advanced Solid Tumors
Active Not Recruiting
A Study of BMS-986442 With Nivolumab With or Without Chemotherapy in Solid Tumors and Non-small Cell Lung Cancer
Terminated
MEM-288 Oncolytic Virus Alone and in Combination With Standard of Care Therapy in Advanced Solid Tumors
Recruiting
A Study of Docetaxel Polymeric Micelles for Injection in Patients With Advanced Solid Tumors
Unknown
A Study to Evaluate the Safety and Efficacy of Docetaxel for Injection (Albumin-bound)in Different Dose Regimens in Patients With Advanced Solid Tumors
Unknown
A Phase II Study of Envofolimab and BD0801 With/Without Chemotherapy in Patients With Advanced Solid Tumors
Terminated
A Study of ASP1570 Taken by Itself, or ASP1570 Taken Together With Either Pembrolizumab, Standard Therapies, or Both, in Adults With Solid Tumors
Terminated
A Phase 1/2 Study of CAN04 in Combination With Different Chemotherapy Regimens in Subjects With Advanced Solid Tumors
Completed
Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of GS-9716 as Monotherapy and in Combination With Anticancer Therapies in Adults With Solid Malignancies
Active Not Recruiting
A Study of OR2805, a Monoclonal Antibody Targeting CD163, Alone and in Combination With Anticancer Agents
Unknown
The Comparison of the Pharmacokinetics of Albumin-bound Docetaxel and Taxotere
Unknown
Study to Assess the Effects of GS-3583 in Participants With Advanced Solid Tumors
Terminated
Evaluation of the Safety and Efficacy of Albumin-bound Docetaxel
Unknown
Safety, PK and Efficacy of ONC-392 in Monotherapy and in Combination of Anti-PD-1 in Advanced Solid Tumors and NSCLC
Active Not Recruiting
Sotorasib Activity in Subjects With Advanced Solid Tumors With KRAS p.G12C Mutation (CodeBreak 101)
Active Not Recruiting
A Study of LY3499446 in Participants With Advanced Solid Tumors With KRAS G12C Mutation
Terminated
A Dose Escalation Study Of PF-06939999 In Participants With Advanced Or Metastatic Solid Tumors
Terminated
ACHP-THP vs EC-THP as Neoadjuvant Therapy for HER2-positive EBC
Active Not Recruiting
Efficacy Study of CPC634 (CriPec® Docetaxel) in Platinum Resistant Ovarian Cancer
Completed
A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults With Relapsed and/or Refractory Solid Tumors
Completed
Study of AG-270 in Participants With Advanced Solid Tumors or Lymphoma With MTAP Loss
Terminated
Risk and Clinical Benefit of Chemotherapy and Intensive Endocrine Therapy for Luminal B1 Early-stage Breast Cancer
Unknown
MEDI5083 Alone and in Combination With Durvalumab, Tremelimumab, and/or Docetaxel.
Completed
An Open-Label Phase I/II Clinical Study of PT-112 in Combination With Docetaxel in Subjects With Advanced Solid Tumor in a Phase I Dose Escalation Study and in Subjects With Non-Small Cell Lung Cancer (NSCLC) in a Phase II Dose Confirmation Study
Unknown
Effect of Chemotherapy vs No Chemotherapy Pre-transplant to MDS Undergoing Allo-HSCT
Unknown
A Study of CriPec® Docetaxel Given to Patients With Solid Tumours
Completed
Study of Pembrolizumab Plus Chemotherapy in Patients With Advanced Cancer (PembroPlus)
Terminated
Curative Study of Chinese Traditional Medicine to Treat Lung Cancer
Unknown
Effects of Fluconazole and Itraconazole CYP3A-Mediated Inhibition on the Pharmacokinetics, Safety, and Tolerability of MLN4924 in Participants With Advanced Solid Tumors
Completed
Clinical Study of Chinese Medicine Plus Chemotherapy Maintenance in Advanced Non Small Cell Lung Cancer
Completed
Sequential Use of Low-dose Sunitinib With Chemotherapy in Advanced NSCLC After Failure of Conventional Regimen
Unknown
Phase I Study of LB-100 With Docetaxel in Solid Tumors
Completed
A Study of HGS1036 in Combination With Chemotherapy in Subjects With Advanced Solid Malignancies
Suspended
Study of ABT-700 in Subjects With Advanced Solid Tumors
Completed
GSK1120212 Rollover Study
Terminated
Safety and Tolerability Study of GSK1120212, a MEK Inhibitor, in Combination With Docetaxel, Erlotinib, Pemetrexed, Pemetrexed + Carboplatin, Pemetrexed + Cisplatin, or Nab-Paclitaxel
Completed
An Extension Protocol for Subjects Who Were Previously Enrolled in Other Tivantinib (ARQ 197) Protocols
Completed
A Phase 1 Study of Alisertib Participants With Advanced Solid Tumors Including Castration-Resistant Prostate Cancer Receiving a Standard Docetaxel Regimen
Completed
A Study of Intravenous Aflibercept With Docetaxel in Chinese Patients With Solid Tumors
Completed
Dose Escalation, Safety and Pharmacokinetic Study of AVE8062 Combined With Docetaxel and Cisplatin in Patients With Solid Tumors
Completed
A Study of the Safety and Efficacy of CNTO 888 in Combination With SoC (Standard of Care) Chemotherapy in Patients With Solid Tumors
Completed
ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Advanced Solid Tumors
Completed
Single Dose Study of [14C]-Labelled AMG 706 in Patients With Advanced Solid Tumors
Completed
Ascending Multiple-Dose Study of Brivanib Alaninate in Combination With Chemotherapeutic Agents in Subjects With Advanced Cancers
Completed
Study Of CP-751,871 In Combination With Sunitinib In Patients With Advanced Solid Tumors
Terminated
A Safety Study in Participants With Advanced Solid Tumors
Terminated
Tailored Neoadjuvant Chemotherapy for Stage II/III Breast Cancer With Tumor Size More Than 2 cm
Completed
Phase 1/2 Study of Vascular Disrupting Agent NPI-2358 + Docetaxel in Patients With Advanced Non-Small Cell Lung Cancer
Completed
Safety of MP470 in Combination With Standard-of-Care Chemotherapy Regimens to Treat Solid Tumors
Completed
Treatment With MK6592 and an Anti-cancer Drug in Patients With Advanced Solid Tumors (6592-001)
Terminated
Study of XIAP Antisense for Advanced Cancers
Terminated
Study of CGC-11047 When Used in Individual Combinations With 1) Gemcitabine or 2) Docetaxel or 3) Bevacizumab or 4) Erlotinib or 5) Cisplatin or 6) 5-Flurouracil or 7) Sunitinib in Patients With Advanced Solid Tumors or Lymphoma
Completed
CP-868,596 And CP-868,596 Plus AG-013736 In Combination With Docetaxel In Advanced Solid Tumors
Completed
To Evaluate the Safety, Tolerability and Pharmacokinetics of AMG 386 When Used in Combination With AMG 706, Bevacizumab, Sorafenib, or Sunitinib.
Completed
A Study to Assess Safety, Tolerability and PK of AZD2171 and Chemotherapy on Patients With Solid Tumors
Completed
A Study of the Proper Dosage of Lovastatin and Docetaxel for Patients With Cancer
Terminated
Study of Suitable Schedule of Docetaxel,Anthracycline and Cyclophosphamide in Adjuvant Therapy of Beast Cancer
Unknown
Thalidomide and Docetaxel in Treating Patients With Advanced Cancer
Completed
Trial of Liposomal Doxorubicin (Doxil) and Weekly Docetaxel (Taxotere)
Completed

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
Docetaxel (this asset)InSilico Medicine Hong Kong LimitedP3B · 62
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 Docetaxel

IndicationSponsorPhaseRating
Prostate NeoplasmP4BBB · 73
Pancreatic AdenocarcinomaP2BBB · 72
Cancer Of Unknown Primary SiteP2BBB · 72

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. Docetaxel 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/docetaxel-cancer

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 →