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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Placebo vials contain 4.5 ml of storage solution only (2.5 ml albumin 20%, 1.1 ml normal saline solution, 0.45 ml Citrate dextrose solution, 0.45 ml Dimethyl sulfoxide). Placebo and MSC vials are indistinguishable in appearance after thawing. There are no observable differences between treatments that could potentially compromise the blind., Mesenchymal stromal cells
Fondazione Telethon ETS
Traumatic Brain Injury
1 trial -
Povorcitinib, Placebo, Povorcitinib, Povorcitinib
Incyte
Treatment of patients with inadequately controlled moderate to severe asthma
1 trial -
Preoperative lanreotide treatment
The First People's Hospital of Lianyungang
Acromegaly
1 trial -
Psilocybin
COGNITION THERAPEUTICS INC
Treatment Resistant Depression
1 trial -
Psilocybin
Compass Therapeutics
Treatment-Resistant Major Depressive Disorder
1 trial -
Psilocybin 25 mg Capsules, TRITTICO 60 mg/ml gocce orali, soluzione, PCB2 (Placebo of psilocybin 25mg), Trazodone placebo (pharmaceutical master preparation prepared according to the Good Pharmacy Practice)
Pari Pharma GmbH
Treatment-resistant depression
1 trial -
RC48- ADC
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Neoadjuvant Treatment of Her2-positive Muscle-invasive Bladder Cance
1 trial -
Radotinib HCl, Placebo for Radotinib HCl
Alphapharm Pty Ltd
Treatment of Parkinson’s disease (PD)
1 trial -
Retifanlimab (INCMGA00012), HOLOXAN 2000 mg, poudre pour usage parentéral, DOXORUBICINE ACCORD 2 mg/ml, solution pour perfusion
The George Institute
Adult patients with treatment-naïve surgically non-metastatic and resectable primary retroperitoneal, limbs and trunk wall undifferentiated pleomorphic sarcomas.
1 trial -
Rixathon 100 mg concentrate for solution for infusion, Aplo-TCSE TCRaß+CD19+ depleto, Allogeneic peripheral blood-derived NK cells CD3- CD56+, Qarziba 4.5 mg/mL concentrate for solution for infusion, Melfalan Tillomed 50 mg polvere e solvente per soluzione iniettabile/infusione, TEPADINA 100 mg powder for concentrate for solution for infusion, Fludarabina Accord 25 mg/ml Concentrato per soluzione iniettabile o per infusione, Grafalon 20 mg/ml concentrato per soluzione per infusione
Istituto Gentili S.r.l.
Patient affected by high risk Neuroblastoma relapsed or in progression after first line treatment.
1 trial -
S-Amlodipine TAB (VAM) 1.25 mg, Amlodipine 2.5 mg
Zentiva k.s.
Patients with moderate or severe oedema on a long-term treatment with amlodipine
1 trial -
SPI-62 as a Treatment for Hypercortisolism Related to a Benign Adrenal Tumor
Lacuna Pharma Pty Ltd
Hypercortisolism related to benign adrenal tumour
1 trial -
Sibeprenlimab, Sibeprenlimab placebo
Otsuka Beijing Research Institute
Treatment of Sjögren’s disease
1 trial -
Sintilimab injection plus Inlyta treatment
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Carcinoma, Renal Cell
1 trial -
Standard Cognitive Behavioral Treatment
BRIGHT MINDS BIOSCIENCES INC.
Substance-Related Disorders
1 trial -
Standard Treatment As Usual (TAU)
BRIGHT MINDS BIOSCIENCES INC.
Substance Abuse
1 trial -
Study evaluating the efficacy of the treatment after targeting PD-L1 and TIGIT in tumors with tertiary lymphoid structures
The George Institute
Adult patients with a histologically confirmed TLS-positive advanced or metastatic NSCLC naïve from systemic treatment or previously treated with chemotherapy and PD1/PDL1 antagonist, and not having previously been treated with CD137 agonists or investigational immune checkpoint blockade therapies, including (but not limited) anti-TIGIT, anti-LAG3. Patients must have adequate organ function with a performance status (WHO 0-1; ECOG 0-1). Patients must not have active or history of autoimmune disease or immune deficiency. The pregnant or breastfeeding women will be excluded. Other eligibility criteria are described in the related section of the protocol.
1 trial -
TAK-653
Takeda
Treatment-Resistant Depression
1 trial -
TEMOZOLOMIDE
Istituto Gentili S.r.l.
Patients with well differentiated neuroendocrine neoplasia (NENs) not eligible for active antitumoral treatments due to their clinical conditions.
1 trial -
TIN816, Sterile 0.9% sodium chloride solution for infusion will be administered as placebo to participants randomized to the placebo treatment. The solution is ready to use in a 100mL infusion bag of 0.9% sodium chloride solution
Novartis Pharmaceuticals
Sepsis associated acute kidney injury
1 trial -
TOPOTECANE ACCORD 1 mg/ml, solution à diluer pour perfusion, VINCRISTINE HOSPIRA 2 mg/2 ml, solution injectable, Etoposide 20 mg/ml concentrate for solution for infusion, CARBOPLATINE HOSPIRA 10 mg/ml, solution injectable pour perfusion, MELPHALAN TILLOMED 50 mg/10 mL, poudre et solvant pour solution injectable / pour perfusion, Topotecan Hospira 4 mg/4 ml concentrate for solution for infusion
The George Institute
Ocular conservative treatment for retinoblastoma
1 trial -
TRASTUZUMAB, TRASTUZUMAB, TRASTUZUMAB EMTANSINE, TRASTUZUMAB, TRASTUZUMAB DERUXTECAN, PERTUZUMAB, TRASTUZUMAB EMTANSINE
Ningbo Cancer Hospital
Patients with HER2-positive locally advanced inoperable or metastatic breast cancer with disease controlled after 2 years of maintenance treatment with anti-HER2 targeted therapy
1 trial -
The treatment group using pembrolizumab combined with anlotinib and radiotherapy and chemotherapy
The First People's Hospital of Lianyungang
Esophageal Cancer
1 trial -
Total Neoadjuvant Treatment
The First People's Hospital of Lianyungang
Biliary Tract Neoplasms
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