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Transoddi (CINAMETIC ACID)

Phase 2 active Small molecule

Transoddi (generic name: CINAMETIC ACID) is a drug. It is currently in Phase 2 development.

Transoddi is thought to work by interacting with specific biological pathways, but the exact mechanism is unknown.

Transoddi, also known as Cinamic Acid, is a small molecule drug with unknown target and drug class. Its commercial status is unclear, and it has not been approved by the FDA for any indications. As a small molecule, it is likely to work by interacting with specific biological pathways, but the exact mechanism is unknown. Further research is needed to determine its safety and efficacy. The lack of information on its pharmacokinetics and pharmacodynamics makes it difficult to assess its potential as a therapeutic agent.

Likelihood of approval
15.3% 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).
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 nameCINAMETIC ACID
ModalitySmall molecule
Therapeutic areaOther
PhasePhase 2

Mechanism of action

Imagine your body's cells are like a complex orchestra, with many different instruments working together to create a beautiful symphony. Transoddi is like a new instrument that is being introduced into the orchestra, but we don't know exactly how it will fit in or what it will sound like. As it interacts with the other instruments, it may help to create a more harmonious and balanced sound, but we need more research to understand how it works.

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

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 Transoddi

What is Transoddi?

Transoddi (CINAMETIC ACID) is a Small molecule drug.

How does Transoddi work?

Transoddi is thought to work by interacting with specific biological pathways, but the exact mechanism is unknown.

What is the generic name of Transoddi?

CINAMETIC ACID is the generic (nonproprietary) name of Transoddi.

What development phase is Transoddi in?

Transoddi is in Phase 2.

Related

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