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
- 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 — searchable for business development and competitive intelligence.
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DEXMEDETOMIDINE , 18F-DPA-714
Pari Pharma GmbH
Patients who survive a COVID ARDS in intensive care must be weaned off invasive mechanical ventilation as quickly as possible. 60% of these patients present with intensive care delirium, a serious event that causes excess mortality and potential acute and late complications, since 30% of patients who present with delirium develop cognitive sequelae. Severe neuroinflammation is considered to be one of the main pathophysiological mechanisms causing delirium during ventilatory weaning. In addition to its sedative properties, dexmedetomidine has neuroprotective effects. In certain experimental models, it reduces cerebral inflammation by acting directly on the microglial phenotype. The role of this chronic neuroinflammatory state on cognitive capacity and reserve is beginning to emerge in the literature, regardless of the initial stress (surgery, head injury or Alzheimer's-type dementia), and is therefore capable of influencing patients' quality of life. The assessment of this neuroinflammation using non-invasive tools would appear to be of prime importance in the management of post-COVID neuro injured patients, as well as the evaluation of potential neuroprotective agents such as dexmedetomidine.
1 trial -
DIFLUPREDNATE, Eylea 40 mg/mL solution for injection in pre-filled syringe, Eylea 40 mg/mL solution for injection in pre-filled syringe, 4D-150, Eylea 40 mg/mL solution for injection in pre-filled syringe, Eylea 40 mg/mL solution for injection in pre-filled syringe
4D Molecular Therapeutics
Macular neovascularization secondary to age-related macular degeneration (nAMD)
1 trial -
DMT310
Dermata Therapeutics
Acne Vulgaris
3 trials -
DNL343
Denali Therapeutics
Amyotrophic Lateral Sclerosis
2 trials -
DOCETAXEL, Inflectra 100 mg powder for concentrate for solution for infusion, Mycofit, 250 mg, kapsułki twarde, DOCETAXEL, INFLIXIMAB, Remsima 100 mg powder for concentrate for solution for infusion, Ceralasertib, MYCOPHENOLATE MOFETIL, Docetaxel Hikma 80 mg/4 ml Konzentrat zur Herstellung einer Infusionslösung, DOCETAXEL, MYCOPHENOLATE MOFETIL, IMFINZI 50 mg/mL concentrate for solution for infusion.
AstraZeneca AB
Advanced or Metastatic Non-Small Cell Lung Cancer
1 trial -
DOTAREM 0,5 mmol/mL, solution injectable, GADOPICLENOL
Guerbet
Suspected Vascular Disease of supra-aortic (carotid/vertebrobasilar), peripheral or abdominal/renal arteries
1 trial -
DOXORUBICIN, Pralatrexate, PREDNISONE, Belinostat, VINCRISTINE SULFATE, CYCLOPHOSPHAMIDE
Lacuna Pharma Pty Ltd
Peripheral T-Cell Lymphoma
1 trial -
DR-3001
Teva Pharma GmbH
Overactive Bladder
1 trial -
Darleukin, Fibromun
Philogen S.p.A.
Malignant melanoma of the skin in patients with locally advanced and fully resectable melanoma with/without prior therapy and presence of injectable cutaneous and/or subcutaneous or nodal lesions
1 trial -
Datopotamab deruxtecan, DOCETAXEL
AstraZeneca AB
TROP2 NMR-positive advanced or metastatic non-squamous non-small cell lung cancer without actionable genomic alterations.
1 trial -
Datopotamab deruxtecan, MYCOPHENOLATE MOFETIL, PEMBROLIZUMAB, INFLIXIMAB, CAPECITABINE, IMFINZI 50 mg/mL concentrate for solution for infusion.
AstraZeneca AB
Stage I-III Triple-negative Breast Cancer with residual invasive disease after neoadjuvant systemic therapy.
1 trial -
Datopotamab deruxtecan, Rilvegostomig, MYCOPHENOLATE MOFETIL, INFLIXIMAB, KEYTRUDA 25 mg/mL concentrate for solution for infusion
AstraZeneca AB
Locally-advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) with high PD-L1 expression (TC ≥ 50%) and without actionable genomic alterations.
1 trial -
Dazodalibep, The placebo is formulated as sterile liquid intended for intravenous infusion following dilution in normal saline. The nominal volume in each vial is 5.0 mL. The placebo is aseptically filled into 6R glass vials, stoppered with a Flurotec-coated elastomeric stopper, and sealed with an aluminum overseal.
Elan Pharma International
Sjögren’s Syndrome With Moderate-toSevere Symptom State
1 trial -
Dazodalibep, The placebo is formulated as sterile liquid intended for intravenous infusion following dilution in normal saline. The placebo is aseptically filled into 6R glass vials( the nominal volume in each vial is 5.0 mL) and 20R glass vials (the nominal volume in each vial is 15.0 mL) , stoppered with a Flurotec-coated elastomeric stopper, and sealed with an aluminum overseal.
Elan Pharma International
Sjögren’s Syndrome With Moderate-to-severe Systemic Disease Activity
1 trial -
Debamestrocel - MSC-NTF (NurOwn)
BRAINSTORM CELL THERAPEUTICS INC.
Amyotrophic Lateral Sclerosis (ALS)
1 trial -
Decartes-08
Cartesian Therapeutics
Myasthaenia Gravis
1 trial -
Deferasirox
Novartis Pharmaceuticals
Transfusion-dependent Iron Overload
1 trial -
Deferiprone oral solution
BRIGHT MINDS BIOSCIENCES INC.
Pantothenate Kinase-Associated Neurodegeneration
1 trial -
Deflazacort
PTC THERAPEUTICS, INC.
Limb-Girdle Muscular Dystrophy
1 trial -
Deflazacort
PTC THERAPEUTICS, INC.
Duchenne Muscular Dystrophy
3 trials -
Delandistrogene moxeparvovec-rokl
Sarepta Therapeutics
Duchenne Muscular Dystrophy
1 trial -
Delayed and extended release mesalazine
Takeda
Colitis, Ulcerative
1 trial -
Dendritic cell immunotherapy
NORTHWEST BIOTHERAPEUTICS INC
Prostate Cancer
1 trial -
Dendritic cell immunotherapy
NORTHWEST BIOTHERAPEUTICS INC
Glioblastoma Multiforme
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 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