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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-, VALSARTAN AND SACUBITRIL , CARVEDILOL , DAPAGLIFLOZIN , -, RAMIPRIL , -, -, LOSARTAN
Pari Pharma GmbH
Heart failure
1 trial -
0.9% Sodium Chloride Solution, Glenzocimab
Pari Pharma GmbH
Acute ischemic stroke
1 trial -
18F-DPA-714
Pari Pharma GmbH
Multiple sclerosis
1 trial -
ACICLOVIR VIATRIS 500 mg, poudre pour solution injectable (I.V.), CHLORURE DE SODIUM 0,9 % B. BRAUN, solution injectable en ampoule
Pari Pharma GmbH
Patients in ICU with invasive mechanical ventilation and HSV throat reactivation with 1 or no organ failures.
1 trial -
ACIDE FOLIQUE CCD 5 mg, comprimé, PLACEBO D'ASPIRINE PROTECT, ASPIRINE PROTECT 100 mg, comprimé gastro-résistant, PLACEBO D'ACIDE FOLIQUE
Pari Pharma GmbH
Patients presenting to ENT emergencies with a unilateral sudden sensorineural hearing loss (SSNHL). SSNHL is defined according to the American ENT society guidelines criteria as a subset of SSNHL that is sensorineural in nature, occurs within a 72 hour window, and consists of a decrease in hearing of ≥30 decibels affecting at least 3 consecutive frequencies: 1. A history of an idiopathic and unilateral sudden decrease in hearing > 72 hours and <15 days. 2. A unilateral sensorineural hearing loss demonstrable on a pure‐tone audiogram at the time of entry into the trial. 3. No other neurological signs except the eight cranial nerve defect; no other types of hearing loss as conductive forms of hearing impairment. 4. No history of fluctuating sensorineural hearing loss or otologic disease.
1 trial -
ACTILYSE 50mg placebo, ACTILYSE, poudre et solvant pour solution injectable et perfusion
Pari Pharma GmbH
intermediate-high-risk acute pulmonary embolism
1 trial -
AMIKACIN
Pari Pharma GmbH
Adult patients admitted to intensive care
1 trial -
AMOXICILLIN TRIHYDRATE, SULFAMETHOXAZOLE AND TRIMETHOPRIM , LEVOFLOXACIN, AMOXICILLIN , AZITHROMYCIN, AZITHROMYCIN , IMMUNOGLOBULINS, NORMAL HUMAN, FOR INTRAVASCULAR ADM., LEVOFLOXACIN
Pari Pharma GmbH
Young Adults and adults with R/R B-cell acute lymphoblastic leukemia (BCP-ALL) or a B cell lymphoma (BCL)
1 trial -
AMOXICILLINE/ACIDE CLAVULANIQUE PANPHARMA 2 g/200 mg ADULTES, poudre pour solution injectable
Pari Pharma GmbH
Intensive care, Ventilator Associated Pneumonia
1 trial -
AZATHIOPRINE, METHYLPREDNISOLONE, PREDNISONE, AZATHIOPRINE, PREDNISOLONE, RITUXIMAB
Pari Pharma GmbH
myelin oligodendrocytes glycoprotein antibody associated diseases (MOGAD)
1 trial -
Ambrisentan Viatris 5 mg film-coated tablets, Placebo de AMBRISENTAN VIATRIS 5 mg - composition: cellulose microcristalline; lactose monohydraté; silice colloïdale anhydre; stéarate de magnésium (vegetable origin); opadry II 85G94065 PINK; eau purifiée, TADALAFIL
Pari Pharma GmbH
Pulmonary arterial hypertension
1 trial -
Aspirin® protect 100 mg Magensaftresistente Tablette Acetylsalicylsäure, Aspirin® protect 300 mg Magensaftresistente Tablette Acetylsalicylsäure, Placebo of Aspirine 100 mg protect, placebo of aspirin 300 mg protect
Pari Pharma GmbH
Colorectal adenomas, Lynch syndrome
1 trial -
BEFIZAL L.P. 400 mg, comprimé enrobé à libération prolongée, BEZAFIBRATE LP 400 mg, BEFIZAL 200 mg, comprimé pelliculé, Placebo BEZAFIBRATE 200 mg
Pari Pharma GmbH
Subjects with PBC with a non-optimal response to UDCA.
1 trial -
BEFIZAL L.P. 400 mg, comprimé enrobé à libération prolongée, placebo of bezafibrate
Pari Pharma GmbH
primary sclerosing cholangitis
1 trial -
BETAMETHASONE, Placebo of fludrocortisone, HYDROCORTISONE HEMISUCCINATE, Placebo of hydrocortisone, FLUDROCORTISONE
Pari Pharma GmbH
Patients admitted to the ICU proven or suspected infection as the main diagnosis.
1 trial -
BOTOX 50 UNITÉS ALLERGAN, poudre pour solution injectable, SODIUM CHLORIDE
Pari Pharma GmbH
Adults aged at least 18 years with painful base-of-thumb osteoarthritis
1 trial -
Bexsero suspension for injection in pre-filled syringe Meningococcal group B Vaccine (rDNA, component, adsorbed), Trumenba suspension for injection in pre-filled syringe Meningococcal group B vaccine (recombinant, adsorbed)
Pari Pharma GmbH
Asplenia
1 trial -
Biological Therapies Sodium Ascorbate Solution 30 g in 100 mL Injection, SODIUM CHLORIDE
Pari Pharma GmbH
Patient with sepsis complicated by ARDS
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 , CEFIXIME , SULFAMETHOXAZOLE AND TRIMETHOPRIM , AMIKACIN
Pari Pharma GmbH
acute pyelonephritis (AP) in children
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 -
CHAMPIX 0.5 mg film-coated tablets, Placebo CHAMPIX ® 0.5mg Comprimé pelliculé
Pari Pharma GmbH
Smokers smoking at least 10 cigarettes/day in the past year
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