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PEX168(200µg)

Jiangsu Hansoh Pharmaceutical Co., Ltd. · Phase 3 active Small molecule ✓ Verified Jun 2026

PEX168(200µg) is a GLP-1 receptor agonist Small molecule drug developed by Jiangsu Hansoh Pharmaceutical Co., Ltd.. It is currently in Phase 3 development for Type 2 diabetes mellitus. Also known as: Polyethylene Glycol Loxenatide.

PEX168 is a long-acting GLP-1 receptor agonist that stimulates insulin secretion and reduces glucagon in response to elevated blood glucose.

PEX168 is a protein modality, specifically a pegylated form of loxenatide, as indicated by its entry in ChEMBL. PEX168(200µg) is one of the doses being studied in clinical trials, including those for Type 2 Diabetes Mellitus and healthy subjects, as listed on ClinicalTrials.gov.

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 namePEX168(200µg)
Also known asPolyethylene Glycol Loxenatide
SponsorJiangsu Hansoh Pharmaceutical Co., Ltd.
Drug classGLP-1 receptor agonist
TargetGLP-1R (GLP-1 receptor)
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 3

Mechanism of action

PEX168 is a pegylated exenatide derivative designed to provide extended duration of action compared to immediate-release GLP-1 agonists. It binds to and activates the GLP-1 receptor on pancreatic beta cells, enhancing glucose-dependent insulin secretion, while simultaneously suppressing glucagon secretion and slowing gastric emptying to improve glycemic control in type 2 diabetes.

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 PEX168(200µg)

What is PEX168(200µg)?

PEX168(200µg) is a GLP-1 receptor agonist drug developed by Jiangsu Hansoh Pharmaceutical Co., Ltd., indicated for Type 2 diabetes mellitus.

How does PEX168(200µg) work?

PEX168 is a long-acting GLP-1 receptor agonist that stimulates insulin secretion and reduces glucagon in response to elevated blood glucose.

What is PEX168(200µg) used for?

PEX168(200µg) is indicated for Type 2 diabetes mellitus.

Who makes PEX168(200µg)?

PEX168(200µg) is developed by Jiangsu Hansoh Pharmaceutical Co., Ltd. (see full Jiangsu Hansoh Pharmaceutical Co., Ltd. pipeline at /company/jiangsu-hansoh-pharmaceutical-co-ltd).

Is PEX168(200µg) also known as anything else?

PEX168(200µg) is also known as Polyethylene Glycol Loxenatide.

What drug class is PEX168(200µg) in?

PEX168(200µg) belongs to the GLP-1 receptor agonist class. See all GLP-1 receptor agonist drugs at /class/glp-1-receptor-agonist.

What development phase is PEX168(200µg) in?

PEX168(200µg) is in Phase 3.

What are the side effects of PEX168(200µg)?

Common side effects of PEX168(200µg) include Nausea, Vomiting, Diarrhea, Injection site reactions.

What does PEX168(200µg) target?

PEX168(200µg) targets GLP-1R (GLP-1 receptor) and is a GLP-1 receptor agonist.

Related

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