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Data updated: Jun 28, 2026

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.

Pharma
OncologyRespiratoryInfectious Disease Execution: Needs Improvement

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. is a pharmaceutical company focused on Oncology, Respiratory, Infectious Disease.

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Since
2
Drugs
-
Trials
0
New Drugs (2yr)

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. at a Glance

  • Growing R&D activity with 59 trials in last 2 years
  • Fast trial execution (19 months median completion)

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s Key Drugs

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s key approved drugs from the last 15 years (excludes generics, biosimilars and IV formulations).

No active drugs

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s Recent FDA Approvals

New NDA/BLA approvals for CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s Therapeutic Areas

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Respiratory. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 73%
0 drugs Phase 3: 17 Phase 2: 26 Phase 1: 51
Respiratory 11%
0 drugs Phase 3: 2 Phase 2: 7 Phase 1: 3
Infectious Disease 6%
0 drugs Phase 2: 4 Phase 1: 6
Metabolic 6%
0 drugs Phase 3: 2 Phase 2: 1 Phase 1: 4
Immunology 5%
0 drugs Phase 2: 4 Phase 1: 3

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s Top Competitors

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD.'s closest competitors by therapeutic-area and drug-target overlap include GSK, Merck, and Johnson & Johnson. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. Pipeline Snapshot

CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. has 130 active clinical programs from ClinicalTrials.gov — 21 Phase 3, 42 Phase 2 and 67 Phase 1.

21
Phase 3
42
Phase 2
67
Phase 1

Phase 3 Readout Calendar Pro

8 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q3 2026
TQF3510 (Semaglutide Injection)
Obesity
Estimated · stale NCT06738979
Q3 2026
TQB2450+Anlotinib
Small Cell Lung Cancer Limited Stage
Estimated · stale NCT06469879
Q4 2026
D-1553 Tablet
Non Small Cell Lung Cancer
Estimated · stale NCT06300177
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Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • Top drug revenue breakdown
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • 8 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 2/23 completed
  • Speed: 19 months avg
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Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges