C4 Therapeutics (CCCC) Evercore ISI 8th Annual HealthCONx Conference summary
Event summary combining transcript, slides, and related documents.
Evercore ISI 8th Annual HealthCONx Conference summary
3 Feb, 2026Clinical program updates
Two active clinical programs: cemsidomide (IKZF1/3 degrader) and CFT8919 (EGFR L858R degrader) are progressing, with cemsidomide moving to the next phase early next year and CFT8919 in a phase one study in China.
Cemsidomide phase one showed a 36% ORR overall, with 40% and 53% ORR at the two highest doses; two complete responses observed at 100 mcg.
Safety profile for cemsidomide is favorable, with no discontinuations due to safety and only 6% dose reductions; most adverse events were not drug-related.
100% of patients were triple-class exposed, and 75% had prior CAR T or T-cell engager therapy; response rates were consistent across these subgroups.
Cemsidomide's efficacy and safety profile compare favorably to mezigdomide, with a more refractory patient population and fewer neutropenic complications.
Regulatory and development plans
No further phase one updates planned for cemsidomide; focus is on advancing to phase two, with an FDA meeting on dose alignment scheduled for later this month.
A prior Type C meeting with the FDA provided feedback shaping current development plans.
The upcoming global 4L+ study will enroll triple-class refractory patients, with a target ORR of around 40% to demonstrate significant improvement over the 20% background rate.
Confidence in single-arm study approval is based on precedent, but regulatory risk remains due to evolving standards and agency personnel.
Commercial and financial outlook
Pricing for cemsidomide is expected to be competitive with current market analogs, but specifics are not disclosed.
Duration of response in late-line settings is currently 9.3 months, exceeding the typical six-month benchmark.
Cash runway extends through the end of 2028, not including up to $40 million in potential milestone payments from partners over 2026–2027.
Key data readouts from the phase two MOMENTUM study are expected by late 2027 (investigator assessment) and later in 2028 (central assessment).
Latest events from C4 Therapeutics
- Cemsidomide and CFT8919 advance as best-in-class degraders for MM and NSCLC, with strong pipeline momentum.CCCC
Corporate presentation13 Mar 2026 - Cemsidomide advances in global trials, targeting best-in-class efficacy for multiple myeloma.CCCC
Barclays 28th Annual Global Healthcare Conference10 Mar 2026 - Cemsidomide advances as a best-in-class myeloma therapy with strong clinical and regulatory momentum.CCCC
TD Cowen 46th Annual Health Care Conference3 Mar 2026 - Advancing next-gen degraders for MM, NSCLC, and INN diseases with strong financial backing.CCCC
Corporate presentation27 Feb 2026 - Cemsidomide advanced in clinical trials, revenue grew, and cash runway extended to 2028.CCCC
Q4 202526 Feb 2026 - Cemsidomide enters late-stage trials with robust financial backing and expedited regulatory strategy.CCCC
Guggenheim Securities Emerging Outlook: Biotech Summit 202611 Feb 2026 - Key data for cemsidomide and CFT1946 expected in H2, supported by strong partnerships and cash runway.CCCC
UBS Targeted Protein Degradation Day 20243 Feb 2026 - Phase 1 programs advance with key data imminent, targeting BRAF resistance and myeloma.CCCC
2024 Wells Fargo Healthcare Conference22 Jan 2026 - CFT1946 shows early efficacy, strong safety, and BRAF degradation in V600 mutant solid tumors.CCCC
Study Update20 Jan 2026