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DRUG CLASS:

Progesterone receptor agonist

Related drugs:
6d
PDCD1 gene single nucleotide polymorphisms and haplotypes are associated with higher risk of breast cancer development. (PubMed, Clin Exp Immunol)
These results indicate that the PDCD1 rs11568821 G>A polymorphism may contribute as a potential susceptibility and prognosis marker for breast cancer, especially for ER+/PR+ subtypes, considering the importance of PD-1 inhibitor effect over anti-tumor response.
Journal • PD(L)-1 Biomarker • IO biomarker
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PD-L1 (Programmed death ligand 1) • ER (Estrogen receptor) • PD-1 (Programmed cell death 1) • PD-L2 (Programmed Cell Death 1 Ligand 2)
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PD-L1 expression
6d
PLATO: Progesterone Levels and Frozen Embryo Transfer Outcomes (clinicaltrials.gov)
P=N/A, N=659, Not yet recruiting, Shady Grove Fertility Reproductive Science Center
New trial
7d
CineP4: Early Luteal Phase Progesterone Kinetics After hCG-Induced Ovulation in Modified Natural Cycle (clinicaltrials.gov)
P=N/A, N=40, Not yet recruiting, University Hospital, Montpellier | Initiation date: Sep 2025 --> Jan 2026
Trial initiation date
7d
Treatment of HRD-positive elderly ovarian cancer patient: a case report. (PubMed, Anticancer Drugs)
Fluzoparib, the domestically developed PARPi in China, has demonstrated significant efficacy in BRCA-mutated ovarian cancer. In the field of supportive care, megestrol acetate (MA) is recommended as the first-line preferred therapeutic agent for cancer-related anorexia by major guidelines, though its role in first-line ovarian cancer therapy remains unexplored, and evidence for its combination with PARPi is lacking...Imaging assessments revealed significant tumor reduction without disease progression or grade ≥3 adverse events observed throughout follow-up. This case highlights the potential of combining PARPi and hormone therapy as a 'chemotherapy-free' precision treatment model for elderly and HRD-positive ovarian cancer patients, offering a promising strategy to balance efficacy and tolerability in a population traditionally underserved by conventional regimens.
Journal • BRCA Biomarker • PARP Biomarker
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BRCA2 (Breast cancer 2, early onset) • HRD (Homologous Recombination Deficiency) • BRCA (Breast cancer early onset)
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HRD • BRCA mutation
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AiRuiYi (fluzoparib) • megestrol
7d
C-HEALTH: Understanding Cycles to Improve Women's Health (clinicaltrials.gov)
P=N/A, N=320, Recruiting, University Hospital, Montpellier | Not yet recruiting --> Recruiting
Enrollment open
10d
FEATS: Failed Endometrial Ablation Treatment With Implantable Progesterone (FEAT) Study (clinicaltrials.gov)
P2, N=0, Withdrawn, Saskatchewan Health Authority - Regina Area | Terminated --> Withdrawn
Trial withdrawal
10d
Potential Biomarkers and Therapeutic Targets of Non-Small Cell Lung Cancer. (PubMed, Altern Ther Health Med)
9 core genes (CCNB1, CCNB2, MAD2L1, BUB1, TTK, CDC20, AURKA, RRM2, GTSE1) were obtained through the KEGG pathway enrichment, which mainly enriched in 4 pathways, namely, Cell cycle, Oocyte meiosis, p53 signaling pathway, and Progesterone-mediated oocyte maturation, respectively. Nine critical dependable DEGs were identified in limited-stage NSCLC using integrated bioinformatical approaches, and these core genes show great potential as prospective biomarkers and therapeutic targets in the progression of limited-stage NSCLC. non-small cell lung cancer, biomarkers, therapeutic targets, p53 signaling pathway, bioinformatics analysis.
Journal
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AURKA (Aurora kinase A) • STING (stimulator of interferon response cGAMP interactor 1) • RRM2 (Ribonucleotide Reductase Regulatory Subunit M2) • CCNB2 (Cyclin B2) • CDC20 (Cell Division Cycle 20) • BUB1 (BUB1 Mitotic Checkpoint Serine/Threonine Kinase) • CCNB1 (Cyclin B1) • MAD2L1 (Mitotic Arrest Deficient 2 Like 1) • GTSE1 (G2 And S-Phase Expressed 1)
13d
Enrollment change
14d
New trial
14d
New P4 trial • Real-world evidence
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megestrol
14d
Lipid-Driven OLR1/FOXM1/FGF19 Axis Orchestrates Crosstalk in an Epithelial-Fibroblast Positive Feedback Promoting Progesterone Resistance in Endometrial Cancer. (PubMed, Adv Sci (Weinh))
Furthermore, treatment with the antioxidant resveratrol (RSV) and its nanoformulation (RSV-NPs) markedly inhibited tumor growth in mice with lipid metabolic disorders, highlighting their potential to counteract progesterone resistance by disrupting this OLR1/FOXM1/FGF19 axis. This work highlights the therapeutic potential of targeting the tumor-stroma metabolic axis to increase progesterone sensitivity and improve outcomes in EC patients with fertility-preserving demands.
Journal
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FGF19 (Fibroblast growth factor 19) • FOXM1 (Forkhead Box M1) • OLR1 (Oxidized Low Density Lipoprotein Receptor 1)
15d
Establishment and Characterization of a New Immortalized Human Adenomyosis Epithelial-Like Cell Line, tAEC21†. (PubMed, Biol Reprod)
In both 2D monolayer and 3D culture, tAEC21 cells responded to 17β-estradiol (E2) but did not respond to progesterone (P4), consistent with the expression of estrogen (ESR1) and progesterone (PGR) receptors. This new epithelial-like, adenomyosis-derived cell line, tAEC21, will be an impactful, biologically plausible research resource.
Preclinical • Journal
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ER (Estrogen receptor) • TERT (Telomerase Reverse Transcriptase) • IL6 (Interleukin 6) • MUC1 (Mucin 1) • TNFA (Tumor Necrosis Factor-Alpha) • CXCL8 (Chemokine (C-X-C motif) ligand 8) • CCL2 (Chemokine (C-C motif) ligand 2) • MME (Membrane Metalloendopeptidase) • CDH2 (Cadherin 2) • KRT5 (Keratin 5)