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Tecemotide

Discontinued / Inactive

Developer: Merck KGaA, Darmstadt, Germany  |  Target Disease: Non-Small Cell Lung Cancer

Program Status: Inactive / Discontinued

Reason: Registry status: TERMINATED

Stage at discontinuation: phase_3

Development Phase Discontinued / Inactive Primary Status
Platform Technology Biological (unspecified platform) Biologic Architecture
Target Indication Non-Small Cell Lung Cancer Pathogen / Antigen
Last Verified 2026-07-10 Tier 1 Multi-Source Checked

Multi-Jurisdiction Regulatory Status

Official licensing, rolling submissions, or authorization status tracked across major health authorities.

Regulatory Authority Status & Details
US FDA Not Filed / Pre-submission
EMA (Europe) Not Filed / Pre-submission
Health Canada Not Filed / Pre-submission
TGA (Australia) Not Filed / Pre-submission

Scientific Profile & Documentation

Platform Architecture
Biological (unspecified platform)
Lead Developer
Merck KGaA, Darmstadt, Germany
Next Expected Milestone
Primary completion (most advanced trial): 2015-06 (registry estimate)
Analyst & Development Notes
Auto-grouped from 2 ClinicalTrials.gov record(s) sharing intervention/sponsor. Phases and timelines are registry fields and may lag company disclosures.
Primary Source Documentation
ClinicalTrials.gov NCT01015443 →
Additional Sources & Literature

Registered Clinical Trials & Studies

Direct registry links to active, completed, or pivotal registration studies across phases.

NCT01015443 Discontinued / Inactive

Cancer Vaccine Study for Stage III, Unresectable, Non-small Cell Lung Cancer (NSCLC) in the Asian Population

Status: Active / OngoingExpected Readout: 2015-06
NCT01423760 Discontinued / Inactive

Common Safety Follow-up Trial of Tecemotide (L-BLP25)

Status: Active / OngoingExpected Readout: 2015-07

Milestone Overview

  • Stage Verification
    Discontinued / Inactive confirmed as of 2026-07-10.
  • Target Milestone
    Primary completion (most advanced trial): 2015-06 (registry estimate)

Vaccine Data Navigator Candidate Profile Registry:

This candidate profile is indexed across all clinical development levels (Preclinical through Phase 1–3, Regulatory Filing, and Licensure) from primary registry databases (ClinicalTrials.gov, WHO ICTRP, FDA CBER, EMA, Health Canada, TGA Australia). Data are updated continuously to track global biologic and vaccine pipelines.