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title: "CX11 | PepTracker Pro"
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# CX11

Medium Evidence 

CX11 is an investigational once-daily oral small-molecule GLP-1 receptor agonist (Corxel/Vincentage) that produced up to 11.5% weight loss at 36 weeks in a 246-patient U.S. Phase 2 obesity trial, with a notably low 12-16% vomiting rate and no hepatic safety signal; global Phase 3 is planned after positive China Phase 3 results.

Aliases CX11 +4 more 

Evidence Medium Evidence 

Last Updated  2026-07-15 

Reading Time  4 min 

## Table of Contents

1.  [What It Is](#what-it-is)
2.  [Regulatory Status](#regulatory-status)
3.  [Why Researchers Study It](#why-researchers-study)
4.  [Proposed Mechanisms](#proposed-mechanisms)
5.  [Evidence Snapshot](#evidence-snapshot)
6.  [Commonly Discussed Benefits](#benefits)
7.  [Safety & Cautions](#safety)
8.  [Comparisons](#comparisons)
9.  [Calculator Tools](#calculator)
10.  [Citations](#citations)

## What It Is

CX11 is an investigational once-daily oral small-molecule (non-peptide) GLP-1 receptor agonist being developed for obesity, overweight, and type 2 diabetes. It was discovered by Vincentage Pharma Co., Ltd. (China), with global ex-China rights acquired by Corxel Pharmaceuticals in December 2024. Like orforglipron, danuglipron, and aleniglipron, CX11 belongs to the emerging class of small-molecule GLP-1 agonists engineered to reproduce the appetite- and glucose-regulating effects of injectable incretin drugs (semaglutide, tirzepatide) in a scalable, room-temperature-stable pill that avoids cold-chain storage and once-weekly injections. On June 23, 2026, Corxel reported positive top-line results from a U.S. Phase 2 trial (NCT07011797) that enrolled 246 adults with obesity (BMI >= 30) or overweight (BMI 27 to <30 with at least one weight-related comorbidity), randomized 1:1:1:1:1 to CX11 120 mg, 160 mg, 200 mg (slow titration), 200 mg (fast titration), or placebo once daily for 36 weeks. CX11 met its primary endpoints, achieving up to 11.5% weight loss at 36 weeks with weight reduction continuing at a consistent rate and no evidence of a slowing (plateauing) trajectory - a pattern suggesting further loss with longer treatment. The tolerability profile was a headline feature: nausea occurred in 33-34% of participants, vomiting in just 12-16%, diarrhea in 4-12%, and constipation in 2-12%, with no severe GI events and GI adverse events concentrated during dose escalation before subsiding during maintenance. The overall discontinuation rate due to GI adverse events was low at 5.0%. Across more than 1,500 participants studied to date (including the China program), no hepatic safety signal has been identified - an important point given that hepatotoxicity concerns ended Pfizer's first oral GLP-1 candidate lotiglipron and complicated twice-daily danuglipron. The U.S. Phase 2 data were described as consistent with the competitive profile established in Vincentage's positive China Phase 3 obesity program. Corxel plans to advance CX11 into pivotal global Phase 3 studies in weight management, and is also developing CX12, an internally discovered oral small-molecule amylin receptor agonist, plus JX10, a thrombolytic for acute ischemic stroke.

Also known as:  CX11, CX-11, Corxel oral GLP-1, Vincentage oral GLP-1 receptor agonist, oral small-molecule GLP-1 RA (Corxel/Vincentage) 

## Regulatory Status

Investigational - not approved 

U.S. Phase 2 trial (NCT07011797) met its primary endpoints in June 2026 with up to 11.5% weight loss at 36 weeks. Partner Vincentage previously reported positive China obesity Phase 3 results. Corxel plans to initiate pivotal global Phase 3 studies in weight management. Not approved for any indication.

Effective: June 2026

[View FDA Source](https://www.biospace.com/press-releases/corxel-pharmaceuticals-reports-positive-top-line-results-from-phase-2-trial-of-cx11-in-obese-and-overweight-u-s-adults)

## Why Researchers Study It

CX11 is part of the wave of oral non-peptide GLP-1 agonists that could dramatically widen access to incretin-based obesity therapy by removing the injection, cold-chain, and manufacturing-scale barriers of peptide drugs. Its Phase 2 profile is of particular interest because it pairs double-digit weight loss with a markedly low vomiting rate and a clean hepatic safety record across >1,500 participants - the two attributes (tolerability and liver safety) that have most often tripped up earlier oral GLP-1 candidates.

## Proposed Mechanisms

-   Small-molecule agonism of the GLP-1 receptor, reducing appetite and caloric intake
-   Delays gastric emptying to promote satiety and reduce food intake
-   Enhances glucose-dependent insulin secretion, supporting glycemic control
-   Non-peptide structure allows once-daily oral dosing without the absorption enhancers or strict fasting requirements of peptide-based oral GLP-1s

## Evidence Snapshot

Medium Evidence 

Low 

Medium 

High 

Study Type

Model

Outcome

Link

Phase 2 (U.S., NCT07011797) - randomized, double-blind, placebo-controlled

246 adults with obesity (BMI >= 30) or overweight (BMI 27 to <30 + comorbidity) - 36 weeks, once-daily oral

Met primary endpoints: up to 11.5% weight loss at 36 weeks with no plateau; low GI burden (nausea 33-34%, vomiting 12-16%, diarrhea 4-12%, constipation 2-12%); 5.0% discontinuation due to GI AEs; no hepatic safety signal

[Source](https://www.biospace.com/press-releases/corxel-pharmaceuticals-reports-positive-top-line-results-from-phase-2-trial-of-cx11-in-obese-and-overweight-u-s-adults)

Phase 3 (China, Vincentage Pharma)

Adults with obesity/overweight - oral CX11

Positive obesity Phase 3 results reported by partner Vincentage; described as establishing the competitive profile confirmed in the U.S. Phase 2 trial

[Source](https://www.biospace.com/press-releases/corxel-pharmaceuticals-reports-positive-top-line-results-from-phase-2-trial-of-cx11-in-obese-and-overweight-u-s-adults)

## Commonly Discussed Benefits

[Weight Management](/benefits/weight-management)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)[Fat Loss](/benefits/fat-loss)[Glycemic Control](/benefits/glycemic-control)

Researching CX11 ? Track it, set reminders, and keep notes in the free app.

[Track in App](https://app.peptrackerpro.com/?add=cx11)

## Safety & Cautions

-   Investigational - not approved for any indication; Phase 2 (U.S.) and Phase 3 (China) completed, global Phase 3 not yet started
-   Top-line results only; full peer-reviewed data and detailed dose-response not yet published
-   GI adverse events (nausea, vomiting, diarrhea, constipation) common, mainly during dose escalation
-   China Phase 3 results reported by the partner rather than in a peer-reviewed journal at time of writing; cross-trial comparisons with orforglipron, aleniglipron, and oral semaglutide have significant limitations
-   Long-term safety, durability of weight loss, and cardiovascular outcomes not yet established

## Comparisons

See how CX11 compares to related peptides:

[CX11 vs Aleniglipron](/compare/cx11-vs-aleniglipron) [CX11 vs Conveglipron](/compare/cx11-vs-conveglipron) [CX11 vs Danuglipron](/compare/cx11-vs-danuglipron) [CX11 vs Ecnoglutide](/compare/cx11-vs-ecnoglutide) [CX11 vs Orforglipron](/compare/cx11-vs-orforglipron) [CX11 vs Semaglutide](/compare/cx11-vs-semaglutide)

## Calculator Tools

Use our research tools to explore dosing and reconstitution data:

[Reconstitution Calculator](/calculators)

## Citations

1.  \[1\]  Corxel Pharmaceuticals Reports Positive Top-Line Results from Phase 2 Trial of CX11 in Obese and Overweight U.S. Adults - BioSpace (June 23, 2026) [PubMed](https://www.biospace.com/press-releases/corxel-pharmaceuticals-reports-positive-top-line-results-from-phase-2-trial-of-cx11-in-obese-and-overweight-u-s-adults)
2.  \[2\]  Corxel to advance oral obesity drug to Phase III trials - Clinical Trials Arena (2026) [PubMed](https://www.clinicaltrialsarena.com/news/corxel-to-advance-oral-obesity-drug-to-phase-iii-trials/)
3.  \[3\]  CX11 Shows Weight Loss in Phase 2 Obesity Trial, Corxel Reports - HCPLive (2026) [PubMed](https://www.hcplive.com/view/cx11-shows-weight-loss-in-phase-2-obesity-trial-corxel-reports)
4.  \[4\]  Corxel gears up for global pivotal push after oral GLP-1 posts 'competitive' phase 2 results - Fierce Biotech (2026) [PubMed](https://www.fiercebiotech.com/biotech/corxel-gears-global-pivotal-push-after-oral-glp-1-posts-competitive-ph-2-results)

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## Related Peptides

### Aleniglipron

Medium Evidence 

An oral non-peptide small-molecule GLP-1 receptor agonist achieving 16.3% placebo-adjusted weight loss at 44 weeks in Phase 2 ACCESS II, with Phase 3 on track for Q3 2026 after positive FDA end-of-Phase 2 feedback.

[Weight Management](/benefits/weight-management)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)[Fat Loss](/benefits/fat-loss)

[View Details](/peptides/aleniglipron) [\+ Compare](/compare?select=aleniglipron)[](https://app.peptrackerpro.com/?add=aleniglipron)

### Conveglipron

Low Evidence 

An oral, once-daily small-molecule GLP-1 receptor agonist (developmental code HDM1002) from Huadong Medicine, in clinical trials for obesity and type 2 diabetes — part of the next wave of GLP-1 'pills' competing with orforglipron.

[Fat Loss](/benefits/fat-loss)[appetite-control](/benefits/appetite-control)[Metabolism](/benefits/metabolism)

[View Details](/peptides/conveglipron) [\+ Compare](/compare?select=conveglipron)[](https://app.peptrackerpro.com/?add=conveglipron)

### Danuglipron

Medium Evidence 

An oral small-molecule GLP-1 receptor agonist discontinued by Pfizer in 2026 after a potential drug-induced liver injury signal, despite showing meaningful weight loss in Phase 2b.

[Weight Management](/benefits/weight-management)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)

[View Details](/peptides/danuglipron) [\+ Compare](/compare?select=danuglipron)[](https://app.peptrackerpro.com/?add=danuglipron)

### Ecnoglutide

High Evidence 

A cAMP signaling-biased GLP-1 receptor agonist approved in China for chronic weight management, with Phase 3 data showing up to 15.4% weight loss.

[Weight Management](/benefits/weight-management)[Fat Loss](/benefits/fat-loss)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)

[View Details](/peptides/ecnoglutide) [\+ Compare](/compare?select=ecnoglutide)[](https://app.peptrackerpro.com/?add=ecnoglutide)

### Orforglipron

High Evidence 

The first oral non-peptide GLP-1 receptor agonist, FDA-approved in April 2026 for chronic weight management with no food or water restrictions.

[Weight Management](/benefits/weight-management)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)[Fat Loss](/benefits/fat-loss)+1 more 

[View Details](/peptides/orforglipron) [\+ Compare](/compare?select=orforglipron)[](https://app.peptrackerpro.com/?add=orforglipron)

### Semaglutide

High Evidence 

A GLP-1 receptor agonist FDA-approved for type 2 diabetes and chronic weight management.

[Weight Management](/benefits/weight-management)[Appetite Regulation](/benefits/appetite-regulation)[Metabolism](/benefits/metabolism)[Fat Loss](/benefits/fat-loss)+3 more 

[View Details](/peptides/semaglutide) [\+ Compare](/compare?select=semaglutide)[](https://app.peptrackerpro.com/?add=semaglutide)

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