Last reviewed · How we verify

Placebo Evogliptin

Eurofarma Laboratorios S.A. · Phase 3 active Small molecule Under review

Placebo Evogliptin is a DPP-4 inhibitor Small molecule drug developed by Eurofarma Laboratorios S.A.. It is currently in Phase 3 development for Type 2 diabetes. Also known as: Placebo.

Evogliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor.

Evogliptin is a small molecule dipeptidyl peptidase IV inhibitor used to treat Type 2 Diabetes. It is classified as an INHIBITOR drug class, specifically targeting the Dipeptidyl peptidase 4 molecular target.

Likelihood of approval
58.3% vs 58.3% industry baseline
If approved by FDA: likely 2028–2030
Steps remaining: NDA/BLA submission
Confidence: High
Why this estimate
  • Baseline phase 3 → approval rate +58.3pp
    Industry-wide phase 3 drugs reach approval ~58.3% 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 2028–2030
EMA EU 2029–2031 +0.7 yr
MHRA GB 2029–2031 +0.7 yr
Health Canada CA 2029–2032 +0.9 yr
TGA AU 2029–2032 +1.2 yr
PMDA JP 2029–2032 +1.5 yr
NMPA CN 2030–2033 +2.3 yr
MFDS KR 2029–2032 +1.4 yr
CDSCO IN 2029–2033 +1.8 yr
ANVISA BR 2030–2033 +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 namePlacebo Evogliptin
Also known asPlacebo
SponsorEurofarma Laboratorios S.A.
Drug classDPP-4 inhibitor
TargetDPP-4
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

DPP-4 inhibitors work by blocking the action of the enzyme DPP-4, which breaks down incretin hormones. This leads to increased levels of incretin hormones, which in turn increases insulin release in response to meals and decreases glucagon levels in the circulation during the postprandial period.

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 Placebo Evogliptin

What is Placebo Evogliptin?

Placebo Evogliptin is a DPP-4 inhibitor drug developed by Eurofarma Laboratorios S.A., indicated for Type 2 diabetes.

How does Placebo Evogliptin work?

Evogliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor.

What is Placebo Evogliptin used for?

Placebo Evogliptin is indicated for Type 2 diabetes.

Who makes Placebo Evogliptin?

Placebo Evogliptin is developed by Eurofarma Laboratorios S.A. (see full Eurofarma Laboratorios S.A. pipeline at /company/eurofarma-laboratorios-s-a).

Is Placebo Evogliptin also known as anything else?

Placebo Evogliptin is also known as Placebo.

What drug class is Placebo Evogliptin in?

Placebo Evogliptin belongs to the DPP-4 inhibitor class. See all DPP-4 inhibitor drugs at /class/dpp-4-inhibitor.

What development phase is Placebo Evogliptin in?

Placebo Evogliptin is in Phase 3.

What are the side effects of Placebo Evogliptin?

Common side effects of Placebo Evogliptin include Hypoglycemia, Nausea, Diarrhea.

What does Placebo Evogliptin target?

Placebo Evogliptin targets DPP-4 and is a DPP-4 inhibitor.

Related

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