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Docetaxel-PM

Sung Yong Oh · Phase 2 active Small molecule

Docetaxel-PM is a Taxane chemotherapy Small molecule drug developed by Sung Yong Oh. It is currently in Phase 2 development for Non-small cell lung cancer, Breast cancer. Also known as: NANOXEL-M, Nanoxel M.

Docetaxel-PM is a taxane chemotherapy medication that works by inhibiting microtubule dynamics, thereby inducing apoptosis in cancer cells.

Docetaxel-PM is a taxane chemotherapy medication that works by inhibiting microtubule dynamics, thereby inducing apoptosis in cancer cells. Used for Non-small cell lung cancer, Breast cancer.

Likelihood of approval
13.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
  • Oncology Phase 2 attrition -2.0pp
    Oncology drugs have higher Phase 2-to-Phase 3 attrition than average — many fail to show OS benefit in larger studies.
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameDocetaxel-PM
Also known asNANOXEL-M, Nanoxel M
SponsorSung Yong Oh
Drug classTaxane chemotherapy
TargetMicrotubules
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 2

Mechanism of action

Docetaxel-PM binds to tubulin and promotes the assembly of microtubules, leading to the stabilization of microtubules and the inhibition of cell division. This results in the induction of apoptosis in rapidly dividing cancer cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Docetaxel-PM

What is Docetaxel-PM?

Docetaxel-PM is a Taxane chemotherapy drug developed by Sung Yong Oh, indicated for Non-small cell lung cancer, Breast cancer.

How does Docetaxel-PM work?

Docetaxel-PM is a taxane chemotherapy medication that works by inhibiting microtubule dynamics, thereby inducing apoptosis in cancer cells.

What is Docetaxel-PM used for?

Docetaxel-PM is indicated for Non-small cell lung cancer, Breast cancer.

Who makes Docetaxel-PM?

Docetaxel-PM is developed by Sung Yong Oh (see full Sung Yong Oh pipeline at /company/sung-yong-oh).

Is Docetaxel-PM also known as anything else?

Docetaxel-PM is also known as NANOXEL-M, Nanoxel M.

What drug class is Docetaxel-PM in?

Docetaxel-PM belongs to the Taxane chemotherapy class. See all Taxane chemotherapy drugs at /class/taxane-chemotherapy.

What development phase is Docetaxel-PM in?

Docetaxel-PM is in Phase 2.

What are the side effects of Docetaxel-PM?

Common side effects of Docetaxel-PM include Neutropenia, Anemia, Thrombocytopenia, Fatigue, Nausea, Vomiting.

What does Docetaxel-PM target?

Docetaxel-PM targets Microtubules and is a Taxane chemotherapy.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing