> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/company/wuhan-createrna-science-and-technology-co-ltd-8f91e894-4109-4867-a9f1-26bbcfb6e70c
> Record changed: 2026-10-13

# Wuhan Createrna Science and Technology Co., Ltd

Registry sponsor category

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Names and classification

**Other names**

- Wuhan Createrna Science and Technology Co., Ltd

**Company name**

Wuhan Createrna Science and Technology Co., Ltd

**Organisation type**

Industry

**Registry sponsor category**

Industry

Source: [clinicaltrials.gov](https://clinicaltrials.gov/)

## Location and listing

**Publicly traded (proxy)**

No

**Listing at source**

Listed

## Related records

### Trials (14)

- A Pharmacokinetic and Safety Study of MY008211A Tablets in Subjects With Impaired or Normal Hepatic Function
- [A Phase II Clinical Study of QR12000 Compound Tablets in Patients With Moderate to Severe Essential Hypertension](https://trialight.com/data/trial/a-phase-ii-clinical-study-of-qr12000-compound-tablets-in-039e8548-5a65-4507-be36-db003c696d2e.md)
- A Study of Multiple Ascending Doses MY008211A in Healthy Adults
- A Study of MY008211A in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
- A Study of Single-dose MY008211A in Healthy Adults
- Effect of Food on Pharmacokinetics of MY008211A Tablets in Healthy Adult Subjects
- Long-term Safety and Tolerability of MY008211A Tablets in Patients With Paroxysmal Nocturnal Hemoglobinuria
- [QR052107B Tablets in Patients With Subacute Cough of Phase Ⅱ Study](https://trialight.com/data/trial/qr052107b-tablets-in-patients-with-subacute-cough-of-phase-77f71d67-205b-40c7-9967-0d56e57649dc.md)
- QR12000 Compound Tablets in Patients with Moderate to Severe Essential Hypertension
- Study of Safety and Efficacy of MY008211A in in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Study of Safety and Efficacy of MY008211A in Paroxysmal Nocturnal Hemoglobinuria (PNH) Patients Who Are Naive to Complement Inhibitor Therapy
- Study of Safety and Efficacy of MY008211A in Patients With Residual Anemia Despite Anti-C5 Antibody Treatment
- Study to Evaluate the Efficacy and Safety of MY008211A in Subjects with Primary Immunoglobulin a Nephropathy (IgAN)
- To Evaluate the Effect of Single Oral Dose of MY008211A Tablets on QTc Interval in Healthy Subjects

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