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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CDZ173/Leniolisib, CDZ173/Leniolisib
Pharming Technologies B.V.
Activated Phosphoinositide 3-Kinase Delta Syndrome
1 trial -
CDZ173/Leniolisib, CDZ173/Leniolisib, CDZ173/Leniolisib
Pharming Technologies B.V.
Activated Phosphoinositide 3-Kinase Delta Syndrome
1 trial -
CEFTAZIDIME, PIPERACILLIN, CEFTAZIDIME AND BETA-LACTAMASE INHIBITOR , CEFTOLOZANE, CEFTAZIDIME, CEFEPIME , CEFEPIME, MEROPENEM , TAZOBACTAM, TAZOBACTAM, MEROPENEM, AMIKACIN , AMIKACIN, PIPERACILLIN AND BETA-LACTAMASE INHIBITOR , CEFTOLOZANE AND BETA-LACTAMASE INHIBITOR , AVIBACTAM, CEFTAZIDIME
Pari Pharma GmbH
antibiotic therapy in Sepsis
1 trial -
CEFTRIAXONE , TEMOCILLIN , Negaban 2 g poudre pour solution injectable/pour perfusion
Pari Pharma GmbH
Neisseria gonorrhoeae Infections
1 trial -
CEFTRIAXONE VIATRIS 1 g, poudre pour solution injectable, Clarithromycine EG 500 mg comprimés pelliculés, MÉTRONIDAZOLE ARROW 500 mg, comprimé pelliculé sécable
Pari Pharma GmbH
Pregnant women with singleton pregnancies hospitalized for threatened late miscarriage with intact membranes
1 trial -
CEFTRIAXONE, AMOXICILLIN, AZITHROMYCIN
Pari Pharma GmbH
Population of study participants Pregnant women with PPROM at 22 to 33 weeks’ gestation
1 trial -
CF101
Can-Fite BioPharma
Keratoconjunctivitis Sicca
2 trials -
CF101
Can-Fite BioPharma
Plaque Psoriasis
1 trial -
CF101 1 mg
Can-Fite BioPharma
Rheumatoid Arthritis
1 trial -
CF101 2mg
Can-Fite BioPharma
Plaque Psoriasis
1 trial -
CG0070 Adenovirus Vector
CG Oncology
Transitional Cell Carcinoma
1 trial -
CGT9486 plus sunitinib
Cogent Biosciences
Advanced Gastrointestinal Stromal Tumors
1 trial -
CHLORURE DE POTASSIUM B. BRAUN 10 % (0,10 g/ml), solution à diluer pour perfusion, GLUCOSE 2,5 % B. BRAUN, solution pour perfusion, MINIRIN 4 microgrammes/ml, solution injectable, SODIUM LACTATE, CHLORURE DE SODIUM 0,9 % AGUETTANT, solution pour perfusion, CHLORURE DE SODIUM HYPERTONIQUE 10 % LAVOISIER, solution à diluer injectable, GLUCOSE 5 % VIAFLO, solution pour perfusion, GADOTERIC ACID
Pari Pharma GmbH
Severe hyponatremia and a high risk of rapid SNa overcorrection
1 trial -
CHLORURE DE SODIUM 0,9 % B. BRAUN, solution injectable en ampoule, TOCILIZUMAB
Pari Pharma GmbH
Sickle cell disease
1 trial -
CHLORURE DE SODIUM 0,9% RENAUDIN, solution injectable, VENLAFAXINE, KETAMINE , 11C-UCB-J
Pari Pharma GmbH
Major depressive disorder with current severe major depressive episode
1 trial -
CHLORURE DE SODIUM FRESENIUS 0,9 %, solution injectable, Tislelizumab
The George Institute
patients with a positive status for molecular residual disease (MRD) [MRD (+)] 2 to 5 months after the end of standard end of standard curative treatment
1 trial -
CI-581a
BRIGHT MINDS BIOSCIENCES INC.
Cocaine Use Disorder
1 trial -
CINRYZE 500
Takeda
Hereditary Angioedema (HAE)
1 trial -
CINRYZE 500 U
Takeda
Hereditary Angioedema (HAE)
1 trial -
CISPLATIN , PACLITAXEL , GEMCITABINE , CARBOPLATIN , placebo for mRNA-4157, PEMETREXED , mRNA-4157, KEYTRUDA 25 mg/mL concentrate for solution for infusion, KEYTRUDA 25 mg/mL concentrate for solution for infusion
Merck Sharp and Dohme
Non-Small Cell Lung Cancer
1 trial -
CISPLATIN, Armisarte 25 mg/ml concentrate for solution for infusion, CARBOPLATIN, PEMETREXED, TAGRISSO 80 mg film-coated tablets, PLACEBO, TAGRISSO 40 mg film-coated tablets
AstraZeneca AB
Patients with histologically or cytologically documented non-squamous NSCLC with completely resectable (Stage II - IIIB N2) disease
1 trial -
CISPLATIN, CARBOPLATIN, IMFINZI 50 mg/mL concentrate for solution for infusion., MYCOPHENOLATE MOFETIL, GEMCITABINE, IMJUDO 20 mg/ml concentrate for solution for infusion., INFLIXIMAB, GEMCITABINE
AstraZeneca AB
Patients with Unresectable Locally Advanced or Metastatic Urothelial Cancer
1 trial -
CISPLATIN, GEMCITABINE, INFLIXIMAB, Rilvegostomig, IMFINZI 50 mg/mL concentrate for solution for infusion., DS-8201a, MYCOPHENOLATE MOFETIL
AstraZeneca AB
Advanced HER2-expressing Biliary Tract Cancer
1 trial -
CISPLATIN, INFLIXIMAB, IMFINZI 50 mg/mL concentrate for solution for infusion., GEMCITABINE, MYCOPHENOLATE MOFETIL
AstraZeneca AB
First-line patients with advanced biliary tract cancers (BTC)
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