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PIPELINE

Product Pipeline

Aoqi's pipeline covers APIs and excipients, finished and semi-finished formulations, technology licensing, and special products for human and animal health. Listed by category below; development status updated as projects advance.

33 products listed13 APIs & Excipients5 Finished & Semi-finished2 Tech Licensing11 Special Products (Human)2 Animal HealthThe GMP column lists the target-market regulatory requirements each line is set up for. Use the category chips above to jump to any table.
API / EXCIPIENT

APIs & Excipients

Product Indication / Use GMP
TirzepatideDiabetes, Obesity
FDANMPA
SemaglutideDiabetes, Obesity
FDANMPA
LiraglutideDiabetes, Obesity
FDANMPA
LinaclotideIrritable Bowel Syndrome (IBS-C) / Chronic idiopathic constipation (CIC)
NMPA
NAD+Anti-aging
NMPAFDA
PenicillamineHeavy metal poisoning / Wilson's disease / Active rheumatoid arthritis
EMANMPA
Dimercaptosuccinic AcidHeavy metal poisoning / Wilson's disease
FDANMPA
RetatrutideDiabetes, Obesity
FDANMPA
TesamorelinWomen Health, ART
FDANMPA
SermorelinWomen Health, ART
FDANMPA
BPC-157Musculoskeletal
FDANMPA
Selank AcetateCNS
FDANMPA
SNACExcipient
EMANMPA
FDF / SEMI-FDF

Finished & Semi-finished Formulations

ProductIndication Dosage TypeType
Linaclotide CapIBS-C / CICCapsule, SemiFDF-particlesGeneric
Semaglutide TabDiabetes, ObesityTablet, SemiFDF-particlesGeneric
Inclisiran InjectionHypercholesterolemiaInjection, API + preparation procedure, API + CMC CROGeneric
Semaglutide CapDiabetes, ObesityCapsule, SemiFDF-particlesInnovative
Tirzepatide CapDiabetes, ObesityCapsule, SemiFDF-particlesInnovative
TECHNOLOGY LICENSE

Technology Licensing

ProductIndication DosageStrength
Tirzepatide CapDiabetes, ObesityCapsule
Semaglutide CapDiabetes, ObesityCapsule5mg, 10mg, 15mg
SPECIAL PRODUCTS

Special Products (Human)

High-barrier generics and complex formulations; development status updated as projects advance.

ProductOriginator IndicationStatus
Cyclosporin Eye Drops (ophthalmic emulsion) 0.05% Single DoseRestasis (Allergan)Dry eye syndromeApproved IND in China, clinical trial developed in China
Azithromycin ophthalmic solution (2.5ml/bottle)AzaSite (Inspire)Bacterial conjunctivitisApproved IND in China, clinical trial developed in China
Vitamin K1 Injection (1MG/0.5ML)AQUAMEPHYTON (Teligent)Vitamin K deficiency bleedingFile in China/US 2025 Q3/Q4
SF6 Microbubble for Injection (59mg/61mg)Sonovue® (Bracco)Ultrasound contrast agentFile in China/US 2026 Q1/Q2
Semaglutide Tablet (3mg/7mg/14mg)Rybelsus (Novo Nordisk)Diabetes, ObesityBE studies in China and Malaysia both finished; approved in Pakistan
Linaclotide Capsules (290μg)Linzess (AstraZeneca)IBS-C, CIC, FCValidation batch finished in China; file in China 2025 Q3
C3F8 Microbubble for Injection (6.52mg/ml, 1.5ml)DEFINITY (Lantheus)Ultrasound contrast agentValidation batch finished in China; filed in China 2025 Q1
Aprocitentan Tablet (12.5mg/25mg)JERAYGO (Idorsia)Resistant hypertensionPilot batch
Rimegepant Tablet (75mg ODT)Nurtec (Pfizer)MigrainePilot batch
Gepotidacin Tablet (750mg)Blujepa (GSK)Urinary tract infectionPilot batch
Baloxavir Marboxil Tablet (20mg, 40mg)Xofluza (Roche, Shionogi)Anti-influenza virusPilot batch
ANIMAL HEALTH

Products for Pet

ProductIndication Status
Lidocaine micropelletAnesthesiaValidation batch / clinical trials
Meloxicam nanocrystallineAnesthesiaValidation batch / clinical trials
PRODUCT FOCUS

Linaclotide Capsule

Guanylate cyclase (GC-C) agonist

ItemDetail
OriginatorIronwood Pharmaceuticals GmbH
Strength & dosage formCapsules 72μg, 145μg, 290μg
Launch regionUS (AbbVie), EMA (AbbVie), China (AstraZeneca), Japan (Astellas)
IndicationIrritable Bowel Syndrome (IBS-C) with constipation; chronic idiopathic constipation (CIC)
PatentAPI expired by 2024; FDF expired by 2029
Launch time2012 in US

Strengths

  • Highly recommended by AGA guidelines for IBS-C, superior to lubiprostone and PEG
  • Best-in-class among guanylate cyclase (GC-C) agonists, superior to plecanatide
  • Broadest indication coverage among novel anti-constipation agents, including adult CIC and functional constipation in children aged 6–17
Cooperation mode
Semi-FDF: particles for capsuleFDF: Capsule
PRODUCT FOCUS

Semaglutide Tablet

SNAC supplied by Aoqi

ItemDetail
OriginatorNovo Nordisk
API / FDFAPI: Aoqi Biotech
Strength & dosage form1.5mg, 4mg, 9mg — Tablet
Launch regionUS, EMA, Japan, China, Korea — more than 50 countries
IndicationDiabetes, Obesity
PatentAPI expired by 2026; FDF by Novo expired by 2033
Launch time2017 in US

Strengths

  • SNAC (supplied by Aoqi) with well-controlled CQAs
  • No restrictions on API preparation process, crystal form or particle size
  • Multiple Rybelsus-generic batches meeting pharmaceutical and bioequivalence, up to 100,000 tablets
  • Dissolution F2 factors: pH 1.2 = 67.69, pH 4.5 = 58.89, pH 6.8 = 65.66
  • Disintegration time and hardness consistent with the RLD

BE study: June 2024, 36 + 36 subjects, single oral dose, three-way crossover, 28-day washout.

Cooperation mode
Semi-FDF: particles for compressionTechnology package: Tech-transfer & SNAC
PRODUCT FOCUS

Semaglutide Capsule (AOAC)

SNAC-free technology package

ItemDetail
Strength & dosage formCapsules 3mg, 5mg, 10mg
IndicationDiabetes, Obesity
PatentAPI expired by 2026; FDF by Novo expired by 2033

Strengths

  • Oral bioavailability is 3× that of Rybelsus; semaglutide dose can be reduced to 1/3
  • No fasting restriction — absorption is independent of gastric pH
  • SNAC-free: supports a 505(b)(2) filing route bypassing the SNAC patent
  • Reduced adverse reactions — intestinal absorption with preclinical and preliminary clinical data suggesting fewer GI side effects

Clinical supply ramp-up: 5,000 capsules Dec 2024 → 20,000 Feb 2025 → 1,000,000 March 2025.

Cooperation mode
Semi-FDF: particles for capsulesTechnology package: Tech-transfer & AOAC

Development status and filing plans shown here are taken from Aoqi product materials for partnering discussion only. Supply, registration and documentation are governed by the executed technical and quality agreements. Chinese names are common translations; INN governs regulatory filings.