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Peil Biomedical Subsidiary Receives NMPA Approval for Phase I Clinical Trial of RA Drug PP011 in China

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Key facts

  • Peil Biomedical Subsidiary Receives NMPA Approval for Phase I Clinical Trial of RA Drug PP011 in China
  • Peil Biomedical announced that its wholly-owned subsidiary, Peil (Shanghai) Pharmaceutical Technology, has received approval from China's National Medical Products Administration (NMPA) to conduct Phase I clinical trials for its oral new drug PP011, intended for rheumatoid arthritis (RA). The trial is expected to be completed by Q1 2027.
  • Source: TWSE
  • Date: Tue Jun 02 2026 09:00:00 GMT+0900 (Japan Standard Time)

Direct answer

Peil Biomedical announced that its wholly-owned subsidiary, Peil (Shanghai) Pharmaceutical Technology, has received approval from China's National Medical Products Administration (NMPA) to conduct Phase I clinical trials for its oral new drug PP011, intended for rheumatoid arthritis (RA). The trial is expected to be completed by Q1 2027.

Citation
Peil Biomedical Subsidiary Receives NMPA Approval for Phase I Clinical Trial of RA Drug PP011 in China (Tue Jun 02 2026 09:00:00 GMT+0900 (Japan Standard Time)), TWSE
Source
TWSE
Date
Tue Jun 02 2026 09:00:00 GMT+0900 (Japan Standard Time)

AI Summary (NQ-processed)

Peil Biomedical announced that its wholly-owned subsidiary, Peil (Shanghai) Pharmaceutical Technology, has received approval from China's National Medical Products Administration (NMPA) to conduct Phase I clinical trials for its oral new drug PP011, intended for rheumatoid arthritis (RA). The trial is expected to be completed by Q1 2027.

AI Analysis

Frequently Asked Questions

Q: What is Peil Biomedical's PP011?
A: It is an oral new drug candidate for rheumatoid arthritis (RA).
Q: What is the clinical trial status?
A: Approved by China's NMPA for Phase I trials, expected to be completed in Q1 2027.
Q: Why develop an oral drug?
A: To address the inconvenience of current injectable biologics for RA treatment.