Intelligence · Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors — phase, modality, and trial IDs for BD and competitive intelligence.
- Programs indexed
- 18,156
- Companies
- 1,062
- Drugs tracked
- 3,187
Quick answer
NovaPharmaNews tracks 18,156 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 — searchable for business development and competitive intelligence.
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SHP465 12.5mg capsules (one capsule daily)
Takeda Pharmaceuticals International AG
Attention Deficit Hyperactivity Disorder (ADHD)
1 trial -
SHP615
Takeda Pharmaceuticals International AG
Nervous System Diseases
2 trials -
SHP640
Takeda Pharmaceuticals International AG
Adenoviral Conjunctivitis
2 trials -
SHP640
Takeda Pharmaceuticals International AG
Bacterial Conjunctivitis
1 trial -
SOTYKTU 6 mg film-coated tablets, Matching Placebo for Deucravacitinib, SOTYKTU 6 mg film-coated tablets, SOTYKTU 6 mg film-coated tablets, ZASOCITINIB, SOTYKTU 6 mg film-coated tablets, Matching Placebo for TAK-279
Takeda Pharmaceuticals International AG
Moderate to Severe Plaque Psoriasis
1 trial -
SPD422 (anagrelide hydrochloride)
Takeda Pharmaceuticals International AG
Essential Thrombocythemia (ET)
1 trial -
SPD465
Takeda Pharmaceuticals International AG
Attention-Deficit/Hyperactivity Disorder
2 trials -
SPD476
Takeda Pharmaceuticals International AG
Ulcerative Colitis
1 trial -
SPD476 (1.2g)
Takeda Pharmaceuticals International AG
Diverticulitis
1 trial -
SPD476 (mesalazine)
Takeda Pharmaceuticals International AG
Colitis, Ulcerative
1 trial -
SPD476 is a polymeric matrix formulation that displays both delayed- and extended-release of mesalazine
Takeda Pharmaceuticals International AG
Ulcerative Colitis
1 trial -
SPD476, MMX™ mesalazine, 1.2g extended release tablet
Takeda Pharmaceuticals International AG
Diverticulitis
1 trial -
SPD489
Takeda Pharmaceuticals International AG
ADHD
1 trial -
SPD489
Takeda Pharmaceuticals International AG
Attention Deficit Hyperactivity Disorder (ADHD)
2 trials -
SPD489
Takeda Pharmaceuticals International AG
Schizophrenia
1 trial -
SPD489 (Lisdexamfetamine dimesylate)
Takeda Pharmaceuticals International AG
Major Depressive Disorder
2 trials -
SPD489 (Lisdexamfetamine dimesylate)
Takeda Pharmaceuticals International AG
Binge Eating Disorder
2 trials -
SPD489 (Lisdexamfetamine dimesylate) + Antidepressant
Takeda Pharmaceuticals International AG
Major Depressive Disorder
1 trial -
SPD489 40mg
Takeda Pharmaceuticals International AG
Schizophrenia
1 trial -
SPD489 Low-Dose
Takeda Pharmaceuticals International AG
Negative Symptoms of Schizophrenia
1 trial -
SPD489 low dose range (40mg, 80mg, and 100mg)
Takeda Pharmaceuticals International AG
Schizophrenia
1 trial -
SPD503 (1 mg)
Takeda Pharmaceuticals International AG
Attention Deficit Disorder With Hyperactivity
1 trial -
SPD503 (Guanfacine hydrochloride)
Takeda Pharmaceuticals International AG
ADHD
1 trial -
SPD503 (Guanfacine hydrochloride) (2 mg)
Takeda Pharmaceuticals International AG
Attention Deficit Disorder With Hyperactivity
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 18,156 clinical development programs grouped by sponsor company, with phase (Phase 1–3), 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 — 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