Intelligence ยท Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors โ phase, modality, and trial IDs for BD and competitive intelligence.
- Programs indexed
- 20,548
- Companies
- 1,769
- Drugs tracked
- 4,797
Quick answer
NovaPharmaNews tracks 20,548 pharmaceutical R&D pipeline programs sourced from ClinicalTrials.gov, linked to sponsor companies. Each profile includes development phase, modality, trial status, NCT identifiers, and indication text โ searchable for business development and competitive intelligence.
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Bioequivalence clinical trial of two formulations of ezetimibe/atorvastatin
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of linagliptin
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of linagliptin
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of linagliptin/metformin.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of loperamide.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of loperamide.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of loperamide.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of loperamide.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence clinical trial of two formulations of rosuvastatin.
Laboratorios Tillomed Spain S.L.U
Hypercholesterolemia
1 trial -
Bioequivalence clinical trial of two formulations of vortioxetine.
Laboratorios Tillomed Spain S.L.U
Healthy volunteers
1 trial -
Bioequivalence study comparing two temazepam 20 mg tablet formulations after fasted administration; an open, randomized, single centre, single dose study with crossover design in healthy subjects
Orion Laboratories Pty.
short-term treatment of insomnia
1 trial -
CKD-393 formulation I
Hong Kong Baptist University
Type II Diabetes
1 trial -
CORT113176 Lipid Capsule Formulation
CORCEPT THERAPEUTICS INC
Healthy Adults
1 trial -
CORT125329 lipid capsule formulation
CORCEPT THERAPEUTICS INC
Healthy
1 trial -
Exploratory Bioavailability of Three Formulations of Gliclazide MR Tablets 120 mg (I.R.I.S.) in Healthy Volunteers Under Fed Conditions (High Fat High Calorie Meal and Standard Meal).
The George Institute
No medical condicion.
1 trial -
HSV 2 Formulation 1
Lxo Ireland Designated Activity Company
Genital Herpes
1 trial -
Lanthanum carbonate Granule Formulation
Takeda
End Stage Renal Disease
1 trial -
MK-7091 Formulations Study in Healthy Adult Participants
Merck Sharp and Dohme
Hypercholesterolemia
1 trial -
Maribavir Commercial Tablet Formulation
Takeda
Healthy Volunteers
1 trial -
Mometasone furoate drug formulation (MFF) 1
BRIGHT MINDS BIOSCIENCES INC.
Hypersensitivity
1 trial -
New formulation
GlaxoSmithKline
Herpes Labialis
1 trial -
Open label, single-center, cross-over randomized, relative bioavailability study comparing a new pitolisant hydrochloride tablet formulation versus the marketed pitolisant (Wakixยฎ) tablet formulation after single oral administrations in healthy subjects.
Bioprojet Pharma
narcolepsy with cataplexy, Narcolepsy
1 trial -
Open label, single-center, cross-over randomized, relative bioavailability study comparing a new pitolisant hydrochloride tablet formulation at 4 different strengths versus the marketed pitolisant (Wakixยฎ) tablet formulation after single oral administrations in healthy subjects
Bioprojet Pharma
Narcolepsy, Narcolepsy with cataplexy
1 trial -
Open label, single-center, two-part pharmacokinetic study: Part I: Relative bioavailability study to compare the pharmacokinetics of BP1.4979 after administration of single oral doses of BP1.4979 as sustained release formulation and actual immediate release formulation, under fasting and fed conditions, in healthy subjects. Part II: Pharmacokinetics of BP1.4979 after a 14-day dosing period with b.i.d. administration of BP1.4979 as sustained release formulation in healthy subjects.
Bioprojet Pharma
Binge eating disorder
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 20,548 clinical development programs grouped by sponsor company, with phase (Phase 1โ3), modality, trial status, and linked NCT IDs from ClinicalTrials.gov.
Where does pipeline data come from?
Program records are derived from ClinicalTrials.gov and linked to NovaPharmaNews company profiles. Trial status and phase reflect registry data at last sync โ verify on ClinicalTrials.gov before investment or partnering decisions. See our data sources page for attribution.
How do I find pipeline programs by company or phase?
Use the search box to match program name, indication, company name, or slug. Results are ordered with late-stage (Phase 3) programs first. Open any row to view the full program profile under its sponsor company.
Data attribution and licensing: Data sources