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cereport

Children's Oncology Group · Phase 1 active Small molecule ✓ Verified May 2026

cereport is a Small molecule drug developed by Children's Oncology Group. It is currently in Phase 1 development. Also known as: labradimil, IND #60315.

Cereport is being studied in clinical trials for various conditions, including brain and central nervous system tumors, meningitis, and HIV infections, in combination with carboplatin and radiation therapy. The exact mechanism of cereport is not specified in the provided information, but it is being investigated in clinical trials for these conditions.

Likelihood of approval
9.6% vs 9.6% industry baseline
If approved by FDA: likely 2033–2036
Steps remaining: Phase 2 → Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 1 → approval rate +9.6pp
    Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2033–2036
EMA EU 2034–2037 +0.7 yr
MHRA GB 2034–2037 +0.7 yr
Health Canada CA 2034–2038 +0.9 yr
TGA AU 2034–2038 +1.2 yr
PMDA JP 2034–2038 +1.5 yr
NMPA CN 2035–2039 +2.3 yr
MFDS KR 2034–2038 +1.4 yr
CDSCO IN 2034–2039 +1.8 yr
ANVISA BR 2035–2039 +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 namecereport
Also known aslabradimil, IND #60315
SponsorChildren's Oncology Group
ModalitySmall molecule
Therapeutic areaOther
PhasePhase 1

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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 cereport

What is cereport?

cereport is a Small molecule drug developed by Children's Oncology Group.

Who makes cereport?

cereport is developed by Children's Oncology Group (see full Children's Oncology Group pipeline at /company/children-s-oncology-group).

Is cereport also known as anything else?

cereport is also known as labradimil, IND #60315.

What development phase is cereport in?

cereport is in Phase 1.

Related

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