Drugs / Rina-S

Trials 9

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/21 trial
Phase 1/2 NCT05579366 Dec 2022 → Jul 2027 expected breast adenocarcinoma, cervical cancer, endometrial cancer, fallopian tube cancer +5 Genmab Recruiting No outcome recorded
Phase 22 trials
Phase 2 NCT07539311 May 2026 → Sep 2028 expected digestive system cancer Genmab Recruiting No outcome recorded
Phase 2 NCT07288177 Jan 2026 → Nov 2027 expected non-small cell lung carcinoma Genmab Recruiting No outcome recorded
Phase 36 trials
Phase 3 NCT07859215 Nov 2026 → Mar 2030 expected ovarian carcinoma Genmab Not yet recruiting No outcome recorded
Phase 3 NCT07564141 Aug 2026 → Dec 2029 expected ovarian cancer Genmab Recruiting No outcome recorded
Phase 3 NCT07604766 Jun 2026 → Sep 2027 expected refractory malignant neoplasm Genmab Recruiting No outcome recorded
Phase 3 NCT07225270 Apr 2026 → Oct 2028 expected ovarian cancer Genmab Recruiting No outcome recorded
Phase 3 NCT07166094 Nov 2025 → Aug 2029 expected endometrial cancer Genmab Recruiting No outcome recorded
Phase 3 NCT06619236 Feb 2025 → Aug 2026 overdue refractory malignant neoplasm Genmab Active not recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2026-10-03 Genmab Results Genmab Announces Rinatabart Sesutecan (Rina-S®) Phase 2 RAINFOL™-01 Results Demonstrated Durable and Clinically Meaningful Responses in Patients with Platinum-Resistant Ovarian Cancer genmab.com ↗
Genmab A/S (Nasdaq: GMAB) today announced results from Part C of the Phase 1/2 RAINFOL™-01 trial evaluating rinatabart sesutecan (Rina-S), an investigational folate receptor alpha (FRα)-targeted, topoisomerase I (TOPO1)-inhibitor antibody-drug conjugate (ADC), demonstrated that among 109 treated patients with platinum-resistant ovarian cancer (PROC), Rina-S achieved a confirmed objective response rate (ORR) of 45.9% (95% CI: 36.3–55.7), including five complete responses (CRs) and a median duration of response (mDOR) of 12.1 months (95% CI: 6.5–15.4), with 51% of responders remaining in response at one year.

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 9 sources stand behind the page.

FieldValueCited text
Known as Rina-S ClinicalTrials.gov intervention name — accepted as the source's own label NCT07225270 ↗
8

NCT07564141 ↗

NCT07604766 ↗

NCT07539311 ↗

NCT07859215 ↗

NCT07166094 ↗

NCT07288177 ↗

NCT06619236 ↗

NCT05579366 ↗

Modality Other / unclassified “a folate receptor alpha (FRα) targeted antibody-drug conjugate” NCT05579366 ↗
Route Intravenous “Intravenous infusion of Rina-S” NCT05579366 ↗