TheraRadar
Home/Indications/Lower respiratory tract infections

Lower respiratory tract infections

0 original drugs
0
Novel Drugs
4
Reformulations
0
Active Trials
0
Drug Targets

Lower respiratory tract infections has 0 FDA-approved novel treatments. Explore market leaders, treatments by mechanism, the clinical pipeline, and drug targets below.

Phase 3 Readouts Pro

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

Full calendar →
Q4 2026
Pirfenidone Capsules (400 mg)
Beijing Continent Pharmaceutical Co, Ltd.
Estimated · fresh NCT07388680
Q4 2026
Meropenem and Pralurbactam
Qilu Pharmaceutical Co., Ltd.
Estimated · aging NCT07089186
Q4 2027
BV100 (300 mg)
BioVersys SAS
Estimated · fresh NCT07326540
Unlock 5 more readouts with confidence-graded estimates
Upgrade to Pro

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.

Lower respiratory tract infections Treatments by Mechanism

Top 5 mechanisms across 8 industry trials with a known mechanism of action.

See full pipeline →
Tetracycline-class Antibacterial
3 trials 2 sponsors
Fluoroquinolone Antibacterial
2 trials 2 sponsors
Interleukin-1 Receptor Antagonist
1 trials 1 sponsor
beta Lactamase Inhibitor
1 trials 1 sponsor
Interleukin-6 Antagonist
1 trials 1 sponsor

MoA derived from FDA pharmClassEpc when intervention matches an approved drug. Codenamed clinical-stage assets without an approved counterpart show "—" and aren't grouped here — they're still in the phase tables below.

Lower respiratory tract infections Clinical Pipeline by Phase

230 industry-sponsored trials across 125 sponsors

Precision Medicine Biomarkers

All biomarkers →

Biomarkers used for patient selection in Lower respiratory tract infections

Novel Lower respiratory tract infections Drugs by Company (New molecular entities)

No novel drugs found for this indication.

Reformulations (4 drugs) Click to expand

Reformulations are FDA-approved versions of existing molecules in new dosage forms (e.g., oral solution vs tablet, extended-release vs immediate-release). They require a new NDA but use an already-proven active ingredient.

Generic Drugs (10 ANDA approved) Click to expand

Drug Categories:

  • Novel Drugs: NDA Type 1/2 (new molecular entity) or original BLA
  • Reformulations: NDA Type 3/5 (new dosage form of existing molecule)
  • Biosimilars: BLA-approved biologics highly similar to reference products
  • Generics: ANDA-approved copies of small molecule drugs

View data sources and methodology