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COMPANY RESEARCH

Salubris

SAL0167 is an internally developed cyclic peptide program for hyperlipidemia that received NMPA clinical trial authorization in 2026. Authorization is not treated as evidence of actual dosing.

Company at a glance

Corporate information

Company entity
深圳信立泰药业股份有限公司
Headquarters / principal office
Futian District, Shenzhen, GuangdongSelf-reported location on the company LinkedIn page; regional scope may differ from the legal or global headquarters. ↗
Founded
1998 ↗
Ownership / capital status
Publicly tradedPublicly traded ↗
Official corporate reference
https://www.salubris.com/en/ ↗
LinkedIn company page
LinkedIn ↗ ↗

Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

SAL0167 is an internally developed cyclic peptide program for hyperlipidemia that received NMPA clinical trial authorization in 2026. Authorization is not treated as evidence of actual dosing.

2026-07-10: Salubris receives trial clearance for cyclic peptide SAL0167 in hyperlipidemia

Program / serviceTarget / indicationRepresentative stageEvidence & scope
SAL0167Lipid lowering; the specific mechanism requires primary-source confirmation · HyperlipidemiaIND clearanceQuantitative human results not confirmed in this review

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

Salubris

Salubris receives trial clearance for cyclic peptide SAL0167 in hyperlipidemia

Salubris announced NMPA clinical-trial clearance for SAL0167 tablets for hyperlipidemia and identified the proprietary candidate as a cyclic peptide. The authorization permits clinical development but does not establish human dosing, quantitative oral exposure, or lipid-lowering efficacy. General statements about cyclic-peptide advantages should not be treated as demonstrated properties of this particular candidate.

Same-field reading (not company-specific)
Johnson & Johnson (PR Newswire)

Icotrokinra meets Phase 3 joint-response endpoint in biologic-naive psoriatic arthritis

Johnson & Johnson reported that 58% of patients receiving icotrokinra 200 mg achieved ACR20 at Week 16 in ICONIC-PsA 1, versus 41% with placebo. The oral IL-23 receptor peptide also showed skin responses. The company reported no new safety signals through Week 24; active psoriatic arthritis remains an investigational indication.

Entera Bio investor filing

Adjacent oral-peptide field: Entera reports $265.9 million cash as EB613 Phase 3 preparations continue

Entera reported $265.9 million in cash and cash equivalents at September 30, plus $6.5 million in restricted cash. Its November 6 update targets first site activation for an approximately 900-patient EB613 osteoporosis Phase 3 trial in late 2026. EB613 is an oral PTH(1-34) program, included here as an adjacent oral-peptide delivery development, not a cyclic-peptide candidate.

Johnson & Johnson

ICONIC-ASCEND reports icotrokinra noninferiority to ustekinumab in plaque psoriasis

Johnson & Johnson reported that ICONIC-ASCEND met its Week 16 co-primary endpoints: PASI 90 responses were 55.2% with icotrokinra versus 3.6% with placebo, and IGA 0/1 responses were 70.4% versus 9.5%. At Week 28, the oral peptide met noninferiority criteria versus ustekinumab across multiplicity-controlled key secondary skin-clearance endpoints.

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Sources & open questions

  • Public information reviewed is insufficient to reconstruct the complete formulation, absolute bioavailability, variability, or food effects.
  1. SAL0167 获临床试验许可 ↗Salubris · 2026-07
  2. Profile ↗Salubris · Not stated
  3. Salubris Pharmaceuticals 公司主页 ↗Salubris/LinkedIn · Not stated
  4. Salubris — official page checked November 4, 2026 ↗Salubris · 2026-11-04 retrieval; original page date retained where shown

Inclusion is not endorsement or partner qualification. Assess company claims, clinical evidence, and project-specific capabilities separately.

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