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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SHR-1701 Combined With Fluazopalil
Hunan Province Tumor Hospital
Non-Small Cell Lung Cancer
1 trial -
SPD489 (lisdexamfetamine dimesylate)
Takeda
Schizophrenia and Predominant Negative Symptoms
1 trial -
SSGJ-705
Sunshine Guojian Pharmaceutical (Shanghai) Co.,
Locally Advanced, Recurrent or Metastatic Malignancies
2 trials -
STRO-002
SUTRO BIOPHARMA, INC.
Neoplasm Malignant
1 trial -
Selinexor
Karyopharm Therapeutics Inc
Solid Tumor Malignancy
1 trial -
Selumetinib
United Therapeutics Europe Ltd
Malignant Peripheral Nerve Sheath Tumors
1 trial -
Sodium chloride Fresenius Kabi 0,9% infuzní roztok, Cerebrolysin 215,2mg/ml Injekční roztok
Lacuna Pharma Pty Ltd
Cerebral Autosomal Dominant Arteriopathy with subcortical Infarcts and Leukoencephalopathy (CADASIL)
1 trial -
SonoVue 8 microlitres/mL powder and solvent for dispersion for injection, CARBOPLATIN
Pari Pharma GmbH
recurrent primary supratentorial malignant brain tumors in children
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-505
Takeda
Malignant Solid Tumors
1 trial -
THOR-707
Sanofi Pasteur
Malignant Melanoma
1 trial -
THYMOGLOBULINE 5 mg/ml, poudre pour solution pour perfusion
The George Institute
haematological malignancies
1 trial -
TL-895, TL-895
Lacuna Pharma Pty Ltd
B Cell Malignancies and Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
1 trial -
TNG908, TNG908, TNG908, TNG908, MIDAZOLAM
Tango Therapeutics
"Ph1: •Locally advanced (LA) or metastatic MTAP-deleted (met.MTAP-del.) solid tumors •MTAP-del.relapsed or refrac. Grade 4 astrocytoma or glioblastoma multiforme (R/R GBM) Ph2: A1:LA or met.MTAP-del. squamous and nonsquamous NSCLC A2:LA or met.MTAP-del. mesothelioma A3:LA or met.MTAP-del. sarcoma A4:LA or met.MTAP-del. pancreatic ductal adenocarcinoma or adenosquamous carcinoma w/predominantly adenocarcinoma histology A5:Other LA or met.MTAP-del. solid tumors A6:MTAP-del. R/R GBM"
1 trial -
TOPOTECAN HYDROCHLORIDE, TOPOTECAN HYDROCHLORIDE, TEMOZOLOMIDE, TEMOZOLOMIDE, TEMOZOLOMIDE, TEMOZOLOMIDE, LEE011, TEMOZOLOMIDE, TEMOZOLOMIDE
Novartis Pharmaceuticals
Relapsed or refractory neuroblastoma and other solid tumors (including medulloblastoma, high grade glioma, malignant rhabdoid tumors, and rhabdomyosarcoma)
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 -
Tecentriq 1 200 mg concentrate for solution for infusion, OXALIPLATINE HOSPIRA 5 mg/ml, solution à diluer pour perfusion, Avastin 25 mg/ml concentrate for solution for infusion., CAPECITABINE VIATRIS 500 mg, comprimé pelliculé
CERO THERAPEUTICS HOLDINGS, INC.
microsatellite stable (MSS) colorectal cancer with liver-dominant metastasis
1 trial -
Testosterone Enanthate 100 MG/ML Injectable Solution
Hospital Authority, Hong Kong
Castration-resistant Prostate Cancer
1 trial -
Thiotepa
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Hematologic Malignancies
1 trial -
Thymalfasin for injection in combination with Recombinant Human Interleukin-2 Injections
The First People's Hospital of Lianyungang
Hematological Malignancy
1 trial -
TransCon TLR7/8 Agonist, TransCon IL-2 ß/ү, KEYTRUDA 25 mg/mL concentrate for solution for infusion
Lacuna Pharma Pty Ltd
Locally advanced or metastatic solid tumor malignancies, platinum resistant ovarian cancer, post-anti-pd-1 melanoma, second line or later cervical cancer, neoadjuvant melanoma and neoadjuvant non-small cell lung cancer, post-anti-pd-L1 non-small cell lung cancer, post-anti-pd-L1 small cell lung cancer, second line or later HER2+ breast cancer
1 trial -
Tremelimumab placebo, concentrate for solution for infusion, Tremelimumab
AstraZeneca AB
unresectable pleural or peritoneal malignant mesothelioma
1 trial -
Ubamatamab
Regeneron UK Limited
SMARCB1-Deficient Malignancies
1 trial -
VK-2019
Cullinan Therapeutics
Nasopharyngeal Carcinoma
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